Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs6795970
SCN10A
0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70 13
rs1057518920
DSP
0.925 0.080 6 7575386 stop gained C/A snv 5
rs104894584
KCNJ2
0.851 0.120 17 70175553 missense variant G/A snv 5
rs199472708
KCNQ1
0.882 0.080 11 2572015 missense variant G/A snv 4
rs1554093433
NKX2-5
0.925 0.080 5 173232833 stop gained G/T snv 4
rs190140598
RYR2
0.851 0.120 1 237445488 missense variant C/A;T snv 1.2E-05 4
rs199473229
SCN5A
0.882 0.120 3 38560361 missense variant A/G snv 4
rs397514616
TNNC1
0.851 0.120 3 52452217 missense variant C/A;T snv 4
rs2824292 0.925 0.080 21 17414857 regulatory region variant G/A snv 0.47 3
rs9388451 0.882 0.120 6 125769231 regulatory region variant T/A;C snv 3
rs192749597
CACNA1C ; CACNA1C-AS1
0.882 0.080 12 2679712 missense variant C/T snv 9.2E-04 3.5E-03 3
rs121912516
KCNH2
0.882 0.120 7 150951721 missense variant C/G snv 3
rs11720524
SCN5A
0.882 0.080 3 38633921 intron variant C/G;T snv 0.34 3
rs12090554
LOC107985239 ; LINC01350
0.925 0.080 1 185583216 intron variant G/A snv 0.15 2
rs1353342
PCSK5
0.925 0.080 9 76259853 intron variant A/C snv 0.79 2
rs199473574
SCN5A
0.925 0.120 3 38603951 missense variant C/T snv 2
rs6125
SELP
0.925 0.080 1 169613079 missense variant C/T snv 5.6E-02 5.2E-02 2
rs188043534
ALG10B
1.000 0.080 12 38316992 missense variant G/T snv 4.0E-06 1