Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs6801957
SCN10A
1.000 0.080 3 38725824 intron variant T/C snv 0.67 5
rs11708996
SCN5A
0.925 0.120 3 38592432 intron variant G/C snv 0.11 5
rs11153730 6 118346359 intergenic variant T/C snv 0.40 4
rs13165478 5 154489480 upstream gene variant G/A snv 0.41 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
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
rs1733724
LNCAROD
10 52464217 intron variant A/G snv 0.82 2
rs9436640
NFIA
1 61408005 intron variant T/G snv 0.44 2
rs6800541
SCN10A
1.000 0.080 3 38733341 intron variant C/T snv 0.70 2
rs991014
SETBP1
18 44859921 intron variant C/T snv 0.35 2
rs11848785
SIPA1L1
14 71590638 intron variant G/A snv 0.82 2
rs2242285
SLC25A26 ; LRIG1
3 66381178 intron variant A/C;G snv 2
rs4687718
TKT
3 53248287 intron variant A/G snv 0.75 2