Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912504
KCNH2
0.851 0.200 7 150951711 missense variant G/A snv 1
rs199473039
KCNH2
0.851 0.120 7 150951512 missense variant G/A;C;T snv 9.5E-05 1
rs199473428
KCNH2
0.851 0.120 7 150951643 missense variant C/A;G;T snv 8.0E-06 1
rs28928905
KCNH2
0.851 0.120 7 150952514 missense variant C/G;T snv 1
rs121912507
KCNH2
0.882 0.120 7 150951511 missense variant C/G;T snv 1
rs121912512
KCNH2
0.882 0.120 7 150950311 missense variant C/T snv 4.0E-06 1.4E-05 1
rs121912516
KCNH2
0.882 0.120 7 150951721 missense variant C/G snv 1
rs199472918
KCNH2
0.882 0.120 7 150951738 missense variant A/G snv 7.2E-05 5.6E-05 1
rs199472921
KCNH2
0.882 0.120 7 150951712 missense variant C/G;T snv 1
rs199472922
KCNH2
0.882 0.120 7 150951708 missense variant T/C;G snv 1
rs199472936
KCNH2
0.882 0.120 7 150951592 missense variant C/A;T snv 1
rs199472944
KCNH2
0.882 0.120 7 150951552 missense variant G/A snv 1
rs199472957
KCNH2
0.882 0.120 7 150951507 missense variant T/A;C;G snv 1
rs199472990
KCNH2
0.882 0.120 7 150950312 missense variant G/A snv 7.0E-06 1
rs199473522
KCNH2
0.882 0.120 7 150951583 missense variant C/T snv 1
rs199473538
KCNH2
0.882 0.120 7 150948981 missense variant G/A snv 4.0E-06 7.0E-06 1
rs36210422
KCNH2
0.882 0.120 7 150958449 missense variant G/A;C snv 3.2E-04 1
rs9333649
KCNH2
0.882 0.200 7 150951679 missense variant C/A;G;T snv 1
rs121912506
KCNH2
0.925 0.120 7 150948984 missense variant C/G;T snv 1
rs121912508
KCNH2
0.925 0.120 7 150951649 missense variant G/A snv 1
rs121912510
KCNH2
0.925 0.120 7 150948995 missense variant G/A snv 4.0E-06 1
rs121912511
KCNH2
0.925 0.120 7 150974825 missense variant T/G snv 1
rs121912514
KCNH2
0.925 0.120 7 150947729 missense variant G/A;T snv 6.0E-05; 6.0E-06 1
rs121912515
KCNH2
0.925 0.120 7 150974720 missense variant G/A;C;T snv 1
rs138776684
KCNH2
0.925 0.120 7 150957380 missense variant G/A snv 1.1E-03 6.3E-04 1