Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs1805128
KCNE1
0.776 0.160 21 34449382 missense variant C/T snv 9.4E-03 10
rs1052536
LIG3
0.776 0.200 17 35004556 3 prime UTR variant C/T snv 0.42 0.36 10
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs3825214
TBX5
0.851 0.080 12 114357638 intron variant G/A snv 0.77 8
rs10494366
LOC105371475 ; NOS1AP
0.851 0.200 1 162115895 intron variant G/T snv 0.54 7
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
rs1415259
NOS1AP ; LOC105371475
0.925 0.080 1 162115519 intron variant C/T snv 0.54 5
rs11153730 6 118346359 intergenic variant T/C snv 0.40 4
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs12143842 0.925 0.160 1 162064100 intergenic variant C/T snv 0.22 3
rs4657139 0.925 0.120 1 162060117 intergenic variant A/T snv 0.48 3
rs9920
CAV1
1.000 0.040 7 116560038 3 prime UTR variant T/C snv 6.7E-02 3
rs11756438
CEP85L
0.925 0.040 6 118672469 intron variant C/A snv 0.42 3
rs7765828
GMPR
6 16294491 intron variant C/G snv 0.56 3
rs12576239
KCNQ1
1.000 0.080 11 2481089 intron variant C/T snv 0.16 3
rs2074238
KCNQ1
1.000 0.120 11 2463573 intron variant T/A;C snv 3
rs246185
MIR193BHG
16 14301575 intron variant T/C snv 0.34 3
rs11710077
SCN5A
3 38616408 intron variant A/T snv 0.17 3
rs3922844
SCN5A
3 38582762 intron variant T/C snv 0.61 3
rs12036340 1 162045950 intergenic variant A/G snv 0.24 2
rs17779747 1.000 0.040 17 70498851 regulatory region variant G/T snv 0.24 2
rs2968863 1.000 0.080 7 150926049 intergenic variant C/T snv 0.16 2