rs121908525
|
0.790 |
0.160 |
2 |
240875159 |
missense variant |
T/C
|
snv
|
4.4E-05
|
5.6E-05
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.860 |
1.000 |
29 |
1991 |
2015 |
rs121908529
|
0.851 |
0.160 |
2 |
240871433 |
missense variant |
G/A;C
|
snv
|
5.6E-04
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.850 |
1.000 |
31 |
1990 |
2019 |
rs121908524
|
0.925 |
0.160 |
2 |
240871379 |
missense variant |
T/A
|
snv
|
9.0E-05
|
1.5E-04
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.820 |
1.000 |
25 |
1991 |
2014 |
rs121908530
|
1.000 |
0.160 |
2 |
240871391 |
missense variant |
G/A;C
|
snv
|
3.1E-05
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
25 |
1991 |
2014 |
rs121908522
|
1.000 |
0.160 |
2 |
240869249 |
missense variant |
G/A
|
snv
|
2.0E-05
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
24 |
1991 |
2014 |
rs121908526
|
1.000 |
0.160 |
2 |
240875125 |
missense variant |
C/T
|
snv
|
5.6E-05
|
4.9E-05
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
24 |
1991 |
2014 |
rs121908527
|
1.000 |
0.160 |
2 |
240875126 |
missense variant |
G/A;C;T
|
snv
|
1.6E-05;
4.0E-06
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
24 |
1991 |
2015 |
rs121908520
|
1.000 |
0.160 |
2 |
240873995 |
missense variant |
T/C
|
snv
|
4.0E-06
|
3.5E-05
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
21 |
1991 |
2014 |
rs536352238
|
1.000 |
0.160 |
2 |
240873987 |
missense variant |
T/A;C
|
snv
|
4.0E-06
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
21 |
1991 |
2014 |
rs121908523
|
0.882 |
0.160 |
2 |
240868986 |
missense variant |
G/A
|
snv
|
1.2E-05
|
4.2E-05
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
20 |
1991 |
2014 |
rs180177197
|
1.000 |
0.160 |
2 |
240869326 |
missense variant |
T/C
|
snv
|
4.0E-06
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
11 |
1998 |
2014 |
rs180177168
|
0.925 |
0.160 |
2 |
240868987 |
missense variant |
G/A;C;T
|
snv
|
4.0E-06
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
10 |
1999 |
2012 |
rs180177225
|
1.000 |
0.160 |
2 |
240871398 |
stop gained |
C/A;T
|
snv
|
4.4E-06;
4.4E-06
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
9 |
2005 |
2015 |
rs180177238
|
1.000 |
0.160 |
2 |
240873014 |
missense variant |
C/T
|
snv
|
4.0E-06
|
2.1E-05
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
9 |
1992 |
2015 |
rs180177156
|
1.000 |
0.160 |
2 |
240878128 |
missense variant |
G/A;T
|
snv
|
4.4E-05;
4.0E-06
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
7 |
1998 |
2015 |
rs180177239
|
1.000 |
0.160 |
2 |
240873022 |
missense variant |
G/A
|
snv
|
4.4E-05
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
7 |
1998 |
2014 |
rs180177253
|
1.000 |
0.160 |
2 |
240874035 |
missense variant |
C/T
|
snv
|
4.0E-06
|
2.1E-05
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
7 |
2003 |
2012 |
rs180177207
|
1.000 |
0.160 |
2 |
240869350 |
missense variant |
G/A
|
snv
|
4.3E-06
|
2.1E-05
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
6 |
1999 |
2014 |
rs180177157
|
1.000 |
0.160 |
2 |
240868971 |
missense variant |
C/T
|
snv
|
4.0E-06
|
2.1E-05
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
5 |
2004 |
2014 |
rs180177227
|
0.882 |
0.160 |
2 |
240871406 |
missense variant |
G/A;C;T
|
snv
|
1.8E-05;
1.3E-05
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
5 |
2006 |
2013 |
rs180177264
|
1.000 |
0.160 |
2 |
240875185 |
missense variant |
T/C
|
snv
|
4.0E-06
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
3 |
2005 |
2012 |
rs180177155
|
1.000 |
0.160 |
2 |
240878086 |
missense variant |
T/A
|
snv
|
4.0E-06
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
2 |
2004 |
2012 |
rs180177173
|
1.000 |
0.160 |
2 |
240869004 |
missense variant |
G/A;C
|
snv
|
2.5E-05;
4.1E-06
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
2 |
2007 |
2012 |
rs180177185
|
1.000 |
0.160 |
2 |
240869248 |
missense variant |
G/C
|
snv
|
4.0E-06
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
2 |
2004 |
2012 |
rs180177222
|
1.000 |
0.160 |
2 |
240871374 |
missense variant |
T/C
|
snv
|
|
|
Primary hyperoxaluria, type I
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.800 |
1.000 |
2 |
2007 |
2012 |