rs1057516430
|
0.925 |
0.120 |
16 |
89811060 |
stop gained |
G/A
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.710 |
1.000 |
1 |
2005 |
2005 |
rs1060501887
|
0.925 |
0.120 |
16 |
89738881 |
splice donor variant |
C/T
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1173704265
|
1.000 |
0.120 |
16 |
89767208 |
missense variant |
A/G
|
snv
|
|
7.0E-06
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
4 |
1997 |
2012 |
rs1184639006
|
1.000 |
0.120 |
16 |
89803333 |
stop gained |
G/A;T
|
snv
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs1188581065
|
1.000 |
0.120 |
16 |
89767140 |
splice donor variant |
C/A
|
snv
|
|
7.0E-06
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1205909298
|
1.000 |
0.120 |
16 |
89767218 |
frameshift variant |
A/-
|
delins
|
|
7.0E-06
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
3 |
1997 |
2009 |
rs1216426444
|
1.000 |
0.120 |
16 |
89764940 |
missense variant |
G/A;T
|
snv
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs121907930
|
1.000 |
0.120 |
16 |
89810716 |
stop gained |
C/T
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1232171121
|
0.925 |
0.120 |
16 |
89814519 |
splice donor variant |
C/A;T
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1247378731
|
1.000 |
0.120 |
16 |
89767213 |
stop gained |
G/A;C;T
|
snv
|
4.0E-06;
1.2E-05;
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
2 |
2005 |
2005 |
rs1278836130
|
1.000 |
0.120 |
16 |
89758648 |
frameshift variant |
T/-
|
del
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs1283284704
|
1.000 |
0.120 |
16 |
89761970 |
stop gained |
-/TCAGGTTGAATTTCCAGCT
|
delins
|
4.0E-06
|
2.1E-05
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
4 |
1997 |
2015 |
rs1285346388
|
1.000 |
0.120 |
16 |
89758702 |
splice acceptor variant |
CTAGAACAGCAAACACTGC/-
|
delins
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
2 |
1997 |
2008 |
rs1291524243
|
0.925 |
0.120 |
16 |
89799203 |
stop gained |
G/A;C
|
snv
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
1 |
2002 |
2002 |
rs1302083447
|
0.925 |
0.120 |
16 |
89764930 |
missense variant |
T/G
|
snv
|
|
7.0E-06
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
4 |
2005 |
2018 |
rs1348367722
|
1.000 |
0.120 |
16 |
89799192 |
frameshift variant |
-/GACT
|
delins
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1365019056
|
1.000 |
0.120 |
16 |
89810706 |
splice donor variant |
C/A
|
snv
|
4.0E-06
|
7.0E-06
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs1381684916
|
1.000 |
0.120 |
16 |
89744993 |
stop gained |
G/A
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
1 |
2005 |
2005 |
rs1388128874
|
1.000 |
0.120 |
16 |
89803342 |
splice acceptor variant |
C/A;G
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs139235751
|
0.925 |
0.120 |
16 |
89775768 |
missense variant |
C/G;T
|
snv
|
2.4E-03;
2.0E-05
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs141422170
|
1.000 |
0.120 |
16 |
89745049 |
missense variant |
G/C
|
snv
|
3.3E-05
|
4.9E-05
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs142833057
|
1.000 |
0.120 |
16 |
89746615 |
missense variant |
G/A;T
|
snv
|
4.8E-05;
2.0E-05
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1429943036
|
1.000 |
0.120 |
16 |
89749805 |
missense variant |
C/A;T
|
snv
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
9 |
1997 |
2008 |
rs1432988639
|
0.925 |
0.120 |
16 |
89740803 |
splice donor variant |
C/A;G;T
|
snv
|
1.2E-05
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs1438828232
|
1.000 |
0.120 |
16 |
89784946 |
stop gained |
G/A
|
snv
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
2 |
2012 |
2013 |