rs1057517481
|
0.925 |
0.240 |
7 |
92494538 |
stop gained |
G/A;C
|
snv
|
4.0E-06
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1057517484
|
0.925 |
0.240 |
7 |
92494614 |
frameshift variant |
-/T
|
delins
|
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1057517484
|
0.925 |
0.240 |
7 |
92494614 |
frameshift variant |
-/T
|
delins
|
|
|
Infantile Refsum Disease (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1057517509
|
0.925 |
0.240 |
7 |
92491472 |
frameshift variant |
TT/-
|
del
|
|
|
Infantile Refsum Disease (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1057517509
|
0.925 |
0.240 |
7 |
92491472 |
frameshift variant |
TT/-
|
del
|
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1057517531
|
0.925 |
0.240 |
7 |
92494398 |
splice acceptor variant |
T/C
|
snv
|
|
|
Infantile Refsum Disease (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1057517531
|
0.925 |
0.240 |
7 |
92494398 |
splice acceptor variant |
T/C
|
snv
|
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs61750426
|
0.925 |
0.240 |
7 |
92494497 |
frameshift variant |
T/-;TTT
|
delins
|
3.6E-05
|
5.6E-05
|
Infantile Refsum Disease (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs759183382
|
0.925 |
0.240 |
7 |
92489894 |
frameshift variant |
GA/-;GAGA
|
delins
|
4.0E-06
|
1.4E-05
|
Infantile Refsum Disease (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs759183382
|
0.925 |
0.240 |
7 |
92489894 |
frameshift variant |
GA/-;GAGA
|
delins
|
4.0E-06
|
1.4E-05
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs762324548
|
0.925 |
0.360 |
7 |
92494491 |
frameshift variant |
T/-
|
del
|
4.0E-06
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs762324548
|
0.925 |
0.360 |
7 |
92494491 |
frameshift variant |
T/-
|
del
|
4.0E-06
|
|
HEIMLER SYNDROME 1
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
|
0.700 |
|
0 |
|
|
rs769836601
|
0.925 |
0.240 |
7 |
92489364 |
frameshift variant |
GACT/-
|
delins
|
2.0E-05
|
1.4E-05
|
Infantile Refsum Disease (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs886043558
|
0.925 |
0.240 |
7 |
92491405 |
frameshift variant |
-/AT
|
delins
|
|
|
Infantile Refsum Disease (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs886043558
|
0.925 |
0.240 |
7 |
92491405 |
frameshift variant |
-/AT
|
delins
|
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs267608179
|
1.000 |
0.240 |
7 |
92494486 |
splice donor variant |
C/T
|
snv
|
2.0E-05
|
5.6E-05
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
1.000 |
7 |
1997 |
2011 |
rs61750429
|
1.000 |
0.120 |
7 |
92494330 |
missense variant |
C/T
|
snv
|
4.0E-06
|
1.4E-05
|
Infantile Refsum Disease (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
4 |
1997 |
2005 |
rs267608180
|
1.000 |
0.240 |
7 |
92494485 |
splice donor variant |
A/G
|
snv
|
8.0E-06
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2001 |
2001 |
rs387907188
|
1.000 |
|
7 |
92448806 |
missense variant |
T/C
|
snv
|
|
|
CARDIOMYOPATHY, DILATED, 2B
|
|
0.800 |
1.000 |
1 |
2011 |
2011 |
rs756151230
|
1.000 |
|
7 |
92470377 |
missense variant |
G/C
|
snv
|
|
|
Human immunodeficiency virus (HIV) II infection category B1
|
|
0.010 |
1.000 |
1 |
2001 |
2001 |
rs1160117945
|
1.000 |
0.240 |
7 |
92489769 |
frameshift variant |
CT/-
|
delins
|
|
7.0E-06
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1554366766
|
1.000 |
0.240 |
7 |
92489724 |
frameshift variant |
C/-
|
del
|
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1554366802
|
1.000 |
0.240 |
7 |
92489771 |
frameshift variant |
T/-
|
del
|
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1554367284
|
1.000 |
0.240 |
7 |
92491271 |
splice donor variant |
C/A
|
snv
|
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1554367358
|
1.000 |
0.240 |
7 |
92491356 |
frameshift variant |
TGGAAGGATCTCGGACATCTCTA/-
|
del
|
|
|
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|