Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs6795970
SCN10A
0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70 13
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 8
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
rs11153730 6 118346359 intergenic variant T/C snv 0.40 4
rs13165478 5 154489480 upstream gene variant G/A snv 0.41 3
rs4642101
CAND2
1.000 0.080 3 12800724 intron variant T/G snv 0.63 3
rs2025096
GSS
20 34952197 5 prime UTR variant G/A snv 0.19 3
rs9912468
PRKCA
17 66322239 intron variant G/A;C snv 3
rs11710077
SCN5A
3 38616408 intron variant A/T snv 0.17 3
rs883079
TBX5
1.000 0.080 12 114355435 3 prime UTR variant C/G;T snv 1.8E-05; 0.61 3
rs10850409 12 114943935 intergenic variant G/A snv 0.27 2
rs12036340 1 162045950 intergenic variant A/G snv 0.24 2
rs1362212 7 35265695 intergenic variant G/A snv 0.11 2
rs17391905 1 51080468 intergenic variant T/G snv 3.7E-02 2
rs7784776 7 46580547 intergenic variant A/G snv 0.42 2
rs9851724 3 38678444 intergenic variant C/T snv 0.73 2
rs4074536
CASQ2
1 115768346 missense variant T/C snv 0.33 0.34 2
rs7562790
CRIM1
2 36446412 intron variant T/G snv 0.48 2
rs17020136
HEATR5B
2 37020872 intron variant T/C snv 0.24 0.18 2
rs1886512
KLF12
13 73946049 intron variant T/A snv 0.40 2