Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060500137
RYR2
1.000 0.080 1 237772077 missense variant G/A snv 1
rs1060500142
RYR2
1.000 0.080 1 237330939 missense variant C/T snv 4.0E-06 1
rs1060502114
TRDN ; TRDN-AS1
1.000 0.080 6 123503894 frameshift variant C/- del 1
rs1060502164
CASQ2
1.000 0.080 1 115744914 splice acceptor variant T/C snv 1
rs1085307100
TRDN
0.925 0.080 6 123512344 frameshift variant -/T delins 2
rs11551437
CALM2
1.000 0.080 2 47161833 missense variant G/A snv 3
rs1185619003
RYR2
1.000 0.080 1 237830557 missense variant A/G snv 1
rs1188352725
RYR2
1.000 0.080 1 237798091 missense variant G/C snv 1
rs1202962809
RYR2
1.000 0.080 1 237784184 missense variant A/C snv 1
rs121434549
CASQ2
0.925 0.080 1 115705212 missense variant C/G;T snv 8.0E-06 2
rs121434550
CASQ2
0.925 0.080 1 115738256 missense variant A/T snv 2
rs1218096653
RYR2
1.000 0.080 1 237828391 missense variant T/G snv 1
rs121918597
RYR2
0.925 0.080 1 237634937 missense variant C/T snv 2
rs121918598
RYR2
0.851 0.080 1 237648523 missense variant G/A;C snv 4
rs121918599
RYR2
0.925 0.080 1 237784024 missense variant C/G snv 2
rs121918600
RYR2
0.882 0.080 1 237791441 missense variant C/T snv 5
rs121918601
RYR2
0.925 0.120 1 237640938 missense variant A/T snv 2
rs121918602
RYR2
0.925 0.120 1 237454396 missense variant T/C snv 3
rs121918603
RYR2
0.882 0.080 1 237639068 missense variant C/T snv 3
rs121918604
RYR2
0.882 0.080 1 237798037 missense variant G/A;T snv 1.7E-05 3
rs121918605
RYR2
0.925 0.080 1 237784314 missense variant A/G snv 2
rs121918606
RYR2
0.925 0.080 1 237819181 missense variant C/G snv 3
rs1234963411
RYR2
1.000 0.080 1 237784188 missense variant A/C snv 1
rs1235005255
RYR2
1.000 0.080 1 237648548 missense variant T/A snv 1
rs1239093704
RYR2
1.000 0.080 1 237759849 missense variant G/T snv 4.0E-06 1