rs876660981
|
1.000 |
0.120 |
20 |
10648632 |
frameshift variant |
AG/-
|
del
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs878853752
|
1.000 |
0.120 |
20 |
10641480 |
frameshift variant |
-/A
|
delins
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs886039393
|
1.000 |
0.120 |
20 |
10645369 |
frameshift variant |
TTTCC/-
|
delins
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs886039887
|
1.000 |
0.120 |
20 |
10644864 |
frameshift variant |
-/T
|
delins
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs886043603
|
1.000 |
0.120 |
20 |
10652513 |
stop gained |
G/A
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs886043606
|
1.000 |
0.120 |
20 |
10663963 |
stop gained |
G/A
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs886044704
|
1.000 |
0.120 |
20 |
10645351 |
splice region variant |
C/G;T
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs930247415
|
1.000 |
0.120 |
20 |
10672709 |
missense variant |
C/T
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs121918351
|
0.882 |
0.240 |
20 |
10658611 |
missense variant |
C/T
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.800 |
1.000 |
17 |
1997 |
2015 |
rs1032920906
|
1.000 |
0.120 |
20 |
10672702 |
missense variant |
G/C
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
14 |
1997 |
2013 |
rs121918350
|
1.000 |
0.120 |
20 |
10658612 |
missense variant |
G/A
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.800 |
1.000 |
14 |
1997 |
2013 |
rs121918352
|
1.000 |
0.120 |
20 |
10672978 |
missense variant |
A/G
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.800 |
1.000 |
14 |
1997 |
2013 |
rs1282498658
|
1.000 |
0.120 |
20 |
10672721 |
missense variant |
G/A
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
14 |
1997 |
2013 |
rs1555829676
|
1.000 |
0.120 |
20 |
10658674 |
missense variant |
G/C
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
14 |
1997 |
2013 |
rs876661122
|
1.000 |
0.120 |
20 |
10641671 |
missense variant |
C/G
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
14 |
1997 |
2013 |
rs876661123
|
1.000 |
0.120 |
20 |
10672991 |
missense variant |
C/T
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
14 |
1997 |
2013 |
rs727504412
|
0.925 |
0.120 |
20 |
10645245 |
frameshift variant |
ACTG/-
|
delins
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
5 |
1997 |
2015 |
rs876660980
|
1.000 |
0.120 |
20 |
10656450 |
stop gained |
G/A;C
|
snv
|
4.0E-06
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
3 |
1998 |
2015 |
rs1437309558
|
1.000 |
0.120 |
20 |
10642587 |
stop gained |
G/A
|
snv
|
4.0E-06
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
2 |
1998 |
2015 |
rs1555827653
|
1.000 |
0.120 |
20 |
10640815 |
frameshift variant |
ACTT/-
|
delins
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
4 |
1999 |
2016 |
rs372984801
|
1.000 |
0.120 |
20 |
10641155 |
stop gained |
G/A;T
|
snv
|
2.4E-05
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
2 |
1999 |
2015 |
rs863223650
|
1.000 |
0.120 |
20 |
10650325 |
missense variant |
C/T
|
snv
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
2 |
2000 |
2012 |
rs1555827769
|
1.000 |
0.120 |
20 |
10641588 |
frameshift variant |
AGGGGTGGACGAAGC/TGCCCTGG
|
delins
|
|
|
Alagille Syndrome 1
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Cardiovascular Diseases
|
0.700 |
1.000 |
1 |
2006 |
2006 |