Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6795970
SCN10A
0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70 13
rs3825214
TBX5
0.851 0.080 12 114357638 intron variant G/A snv 0.77 8
rs6801957
SCN10A
1.000 0.080 3 38725824 intron variant T/C snv 0.67 7
rs11708996
SCN5A
0.925 0.120 3 38592432 intron variant G/C snv 0.11 6
rs6730558
LOC105373411
2 8616053 intron variant C/T snv 0.47 5
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 4
rs17287293
LOC105369698
1.000 0.080 12 24617944 intergenic variant A/G snv 0.12 4
rs12127701
MYBPHL
1 109295642 intron variant A/G snv 6.2E-02 4
rs882300
LOC107985947
1.000 0.080 2 136218685 intergenic variant T/C;G snv 3
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 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
rs3922844
SCN5A
3 38582762 intron variant T/C snv 0.61 3
rs7312625
TBX5
1.000 0.080 12 114362169 intron variant G/A snv 0.71 3
rs11264339 1.000 0.040 1 155168172 downstream gene variant C/T snv 0.56 2
rs251253 1.000 0.040 5 173053333 upstream gene variant C/T snv 0.51 2
rs3807989
CAV1
1.000 0.080 7 116546187 intron variant A/G snv 0.53 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
rs7729395
PAM
1.000 0.080 5 102764872 intron variant C/T snv 3.1E-02 2
rs6599255
SCN10A
3 38754924 intron variant A/C;T snv 2
rs6798015
SCN10A
1.000 0.080 3 38757345 intron variant C/T snv 0.70 2
rs12053903
SCN5A
3 38551902 intron variant T/C snv 0.49 2
rs1895582
TBX5
12 114369230 intron variant G/A snv 0.70 2
rs12678719
ZFPM2
1.000 8 105503826 intron variant C/G snv 0.37 2