Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10494366
LOC105371475 ; NOS1AP
0.851 0.200 1 162115895 intron variant G/T snv 0.54 7
rs11708996
SCN5A
0.925 0.120 3 38592432 intron variant G/C snv 0.11 6
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs137854600
SCN5A
0.807 0.120 3 38551504 missense variant C/A;T snv 6
rs199473225
SCN5A
0.851 0.120 3 38560397 missense variant G/A;C snv 6
rs1064794243
SCN4A
0.851 0.200 17 63941169 missense variant A/T snv 5
rs137854607
SCN5A
0.882 0.120 3 38554309 missense variant C/G;T snv 5
rs137854612
SCN5A
0.851 0.120 3 38560170 missense variant C/T snv 4
rs137854615
SCN5A
0.851 0.120 3 38550989 missense variant A/G snv 4
rs199473229
SCN5A
0.882 0.120 3 38560361 missense variant A/G snv 4
rs199473556
SCN5A
0.851 0.120 3 38630342 missense variant G/A snv 4
rs72549410
SCN5A
0.851 0.120 3 38606058 missense variant C/T snv 4
rs79299226
SCN5A
0.851 0.120 3 38550898 missense variant A/G snv 4
rs137854613
SCN5A
0.882 0.120 3 38551505 stop gained G/A;T snv 3
rs137854614
SCN5A
0.882 0.120 3 38550988 missense variant T/C snv 3
rs199473092
SCN5A
0.925 0.080 3 38608175 missense variant A/C snv 3
rs199473096
SCN5A
0.882 0.120 3 38606751 missense variant G/A snv 3
rs199473143
SCN5A
0.925 0.080 3 38597949 missense variant T/G snv 3
rs199473207
SCN5A
0.882 0.120 3 38566555 missense variant G/A snv 3
rs199473311
SCN5A
0.882 0.120 3 38551070 missense variant T/C snv 7.0E-06 3
rs727504801
SCN5A
0.925 0.080 3 38560397 frameshift variant G/- delins 3
rs9388451 0.882 0.120 6 125769231 regulatory region variant T/A;C snv 3
rs10428132
SCN10A
0.925 0.120 3 38736063 intron variant T/G snv 0.67 2
rs1237724419
SCN5A
0.925 0.080 3 38575390 stop gained C/A;T snv 2
rs199473093
SCN5A
0.925 0.080 3 38606802 missense variant G/A snv 2