Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4743034
ZNF462
1.000 0.080 9 106870072 intron variant G/A snv 0.27 3
rs4830542
ACE2
0.925 0.080 X 15558483 downstream gene variant C/G;T snv 3
rs6666258
KCNN3
0.882 0.080 1 154841792 intron variant G/C snv 0.30 3
rs6790396
SCN10A
1.000 0.080 3 38730434 intron variant C/G snv 0.67 3
rs6800541
SCN10A
1.000 0.080 3 38733341 intron variant C/T snv 0.70 3
rs6817105 0.882 0.080 4 110784612 intergenic variant T/C snv 0.19 3
rs7312625
TBX5
1.000 0.080 12 114362169 intron variant G/A snv 0.71 3
rs749547712
CASQ2
0.882 0.080 1 115768444 missense variant C/T snv 1.2E-05 3
rs755492182
ACTN2
0.882 0.080 1 236735677 missense variant C/T snv 3
rs7612445 1.000 0.080 3 179455191 upstream gene variant G/T snv 0.24 3
rs7629265
SCN5A
0.882 0.080 3 38607330 intron variant C/T snv 2.3E-02 3
rs883079
TBX5
1.000 0.080 12 114355435 3 prime UTR variant C/G;T snv 1.8E-05; 0.61 3
rs9899183
TNFSF12-TNFSF13 ; TNFSF12
1.000 0.080 17 7549660 intron variant C/G;T snv 3
rs1044258
ARMH3 ; LOC107984029
1.000 0.080 10 101845957 3 prime UTR variant T/C snv 0.26 2
rs10786662
PITX3 ; ELOVL3
1.000 0.080 10 102230055 downstream gene variant G/C snv 0.58 2
rs10842383
LOC105369698
1.000 0.080 12 24619033 intergenic variant C/T snv 0.11 2
rs11047543
LOC105369698
1.000 0.080 12 24635405 intergenic variant G/A snv 0.12 2
rs1131691325
GATA4
0.925 0.080 8 11749042 missense variant T/C snv 4.0E-06 2
rs1131820
KCNN3
0.925 0.080 1 154772376 synonymous variant A/G snv 0.77 0.71 2
rs113710653
SPATC1L
0.925 0.080 21 46161921 missense variant C/T snv 6.5E-02 6.1E-02 2
rs12044963
KCND3
1.000 0.080 1 111849738 intron variant G/T snv 0.10 2
rs121908593
KCNA5
0.925 0.080 12 5045975 missense variant G/A snv 8.0E-06 7.0E-06 2
rs1278493
PPP2R3A
1.000 0.080 3 136095167 intron variant G/A;C snv 2
rs13072552
CP
1.000 0.080 3 149195339 intron variant G/T snv 0.18 2
rs13376333
KCNN3
0.925 0.080 1 154841877 intron variant C/T snv 0.28 2