Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs794728708
RYR2
0.827 0.120 1 237377386 missense variant G/A;T snv 8
rs267607277
CALM1
0.807 0.120 14 90404386 missense variant A/G snv 6
rs398124647
CALM2
0.807 0.120 2 47161851 missense variant T/A;C snv 6
rs121918600
RYR2
0.882 0.080 1 237791441 missense variant C/T snv 5
rs121918598
RYR2
0.851 0.080 1 237648523 missense variant G/A;C snv 4
rs11551437
CALM2
1.000 0.080 2 47161833 missense variant G/A snv 3
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
rs121918606
RYR2
0.925 0.080 1 237819181 missense variant C/G snv 3
rs1273246817
RYR2
0.882 0.080 1 237784169 missense variant A/C snv 3
rs1458500258
RYR2
0.925 0.080 1 237388098 missense variant G/T snv 7.0E-06 3
rs398124650
CALM2
0.882 0.120 2 47161744 missense variant C/G;T snv 3
rs794728721
RYR2
0.925 0.080 1 237445489 missense variant G/A snv 3
rs1085307100
TRDN
0.925 0.080 6 123512344 frameshift variant -/T delins 2
rs121434550
CASQ2
0.925 0.080 1 115738256 missense variant A/T snv 2
rs121918597
RYR2
0.925 0.080 1 237634937 missense variant C/T snv 2
rs121918599
RYR2
0.925 0.080 1 237784024 missense variant C/G snv 2
rs121918601
RYR2
0.925 0.120 1 237640938 missense variant A/T snv 2
rs121918605
RYR2
0.925 0.080 1 237784314 missense variant A/G snv 2
rs1401116572
RYR2
1.000 0.080 1 237441382 missense variant G/A snv 2
rs1415931588
RYR2
1.000 0.080 1 237377426 missense variant A/T snv 2
rs267607276
CALM1
0.925 0.080 14 90401385 missense variant A/G;T snv 2
rs398124648
CALM2
0.925 0.080 2 47161748 missense variant A/C snv 2
rs398124649
CALM2
0.925 0.080 2 47161737 missense variant T/G snv 2
rs730880199
RYR2
0.925 0.080 1 237819167 missense variant T/G snv 2