Gene: ABCC8 ×
Source: CLINVAR ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs193922401
rs193922401
ABCC8
1 1.000 0.120 11 17395914 missense variant C/A;T snv 0.710 1.000 0 2007 2007
dbSNP: rs141322087
rs141322087
ABCC8
13 0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs193922396
rs193922396
ABCC8
1 1.000 0.120 11 17442744 missense variant A/G snv 0.700 0
dbSNP: rs193922397
rs193922397
ABCC8
1 1.000 0.120 11 17442734 missense variant T/C snv 4.0E-06 0.700 0
dbSNP: rs193922399
rs193922399
ABCC8
1 1.000 0.120 11 17404527 missense variant A/C snv 0.700 0
dbSNP: rs193922400
rs193922400
ABCC8
2 0.925 0.120 11 17404524 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs193922403
rs193922403
ABCC8
1 1.000 0.120 11 17395215 missense variant G/A;C snv 1.9E-04 0.700 0
dbSNP: rs193922406
rs193922406
ABCC8
1 1.000 0.120 11 17393752 missense variant A/C snv 0.700 0
dbSNP: rs193922407
rs193922407
ABCC8
1 1.000 0.120 11 17393741 missense variant C/T snv 0.700 0
dbSNP: rs193922408
rs193922408
ABCC8
2 0.925 0.120 11 17393122 missense variant C/T snv 0.700 0