Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11153730 6 118346359 intergenic variant T/C snv 0.40 4
rs11710077
SCN5A
3 38616408 intron variant A/T snv 0.17 3
rs246185
MIR193BHG
16 14301575 intron variant T/C snv 0.34 3
rs3922844
SCN5A
3 38582762 intron variant T/C snv 0.61 3
rs7765828
GMPR
6 16294491 intron variant C/G snv 0.56 3
rs12036340 1 162045950 intergenic variant A/G snv 0.24 2
rs12053903
SCN5A
3 38551902 intron variant T/C snv 0.49 2
rs16857031
NOS1AP ; LOC105371475
1 162143120 intron variant C/G snv 0.18 2
rs2298632
TCEA3
1 23383982 3 prime UTR variant C/T snv 0.40 2
rs2968864 7 150925074 intergenic variant T/C snv 0.16 2
rs6845865
ARHGAP10
4 148053451 intron variant T/C snv 0.27 2
rs727957
KCNE1
21 34507774 intron variant G/A;T snv 2
rs728926
KLF12
13 73938985 intron variant C/T snv 0.34 2
rs9892651
PRKCA
17 66307675 intron variant C/T snv 0.59 2
rs10040989 5 138238036 intergenic variant G/A snv 0.12 1
rs10127719
NOS1AP
1 162186380 intron variant T/A;C snv 1
rs10432489
SCHLAP1
2 180813076 intron variant A/C;G snv 1
rs10482996
LOC105372770 ; BACH1
21 29492492 intron variant C/T snv 7.6E-02 1
rs10775360 17 70329727 intron variant C/T snv 0.25 1
rs10800352
NOS1AP
1 162202899 intron variant A/G snv 0.27 1
rs10819861
ERCC6L2
9 96105531 intron variant T/A;C snv 1
rs10918602
NOS1AP
1 162067910 upstream gene variant T/C snv 0.25 1
rs10919070
ATP1B1
1 169129799 intron variant A/C snv 0.10 1
rs10919071
ATP1B1
1 169130245 intron variant A/G snv 0.10 1
rs1106399 2 200139114 regulatory region variant A/C snv 0.15 1