Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs4657139 0.925 0.120 1 162060117 intergenic variant A/T snv 0.48 3
rs1047624774
ATP2B4
1.000 0.120 1 203700807 missense variant T/C snv 4.0E-06 3.5E-05 2
rs10800397
NOS1AP
1.000 0.120 1 162267300 intron variant C/G;T snv 1
rs779760381
SLC2A5
1.000 0.120 1 9039877 missense variant G/A snv 1.2E-05 1
rs398124647
CALM2
0.807 0.120 2 47161851 missense variant T/A;C snv 6
rs11551462
CALM2
0.925 0.120 2 47160802 missense variant A/G snv 2
rs41261344
SCN5A
0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 11
rs137854601
SCN5A
0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs72546668
SSUH2 ; CAV3
0.807 0.200 3 8745644 missense variant C/A;T snv 4.0E-06; 2.6E-03 8
rs116840778
SSUH2 ; CAV3
0.882 0.200 3 8733956 missense variant G/A;C snv 7
rs137854600
SCN5A
0.807 0.120 3 38551504 missense variant C/A;T snv 6
rs12720452
SCN5A
0.882 0.120 3 38603758 missense variant C/T snv 2.9E-04 2.9E-04 5
rs199473282
SCN5A
0.827 0.120 3 38551513 missense variant G/A;T snv 4.0E-06 5
rs137854615
SCN5A
0.851 0.120 3 38550989 missense variant A/G snv 4
rs199473124
SCN5A
0.851 0.120 3 38603902 missense variant A/T snv 8.0E-06 7.0E-06 4
rs199473604
SCN5A
0.882 0.120 3 38560394 missense variant G/T snv 4
rs28936686
SSUH2 ; CAV3
0.851 0.200 3 8745688 missense variant G/A;T snv 1.6E-04; 2.0E-05 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
rs104893714
SSUH2 ; CAV3
0.925 0.120 3 8745701 missense variant T/G snv 3
rs137854614
SCN5A
0.882 0.120 3 38550988 missense variant T/C snv 3
rs199473096
SCN5A
0.882 0.120 3 38606751 missense variant G/A snv 3
rs199473133
SCN5A
0.882 0.120 3 38603747 missense variant G/A snv 3.1E-05 6.3E-05 3
rs199473311
SCN5A
0.882 0.120 3 38551070 missense variant T/C snv 7.0E-06 3