Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs414171
MAPKAPK3 ; CISH
0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 3
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 3
rs199473565
SCN5A
0.882 0.120 3 38606743 missense variant C/T snv 4.0E-06 7.0E-06 2
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 1
rs763809932
TTN ; TTN-AS1
1.000 0.080 2 178614110 missense variant G/A;T snv 2.4E-05 1.4E-05 1