Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs76863441
PLA2G7
0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs1157637439
VARS2
0.882 0.120 6 30920187 missense variant A/G snv 4
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs121908991
PRKAG2
0.807 0.120 7 151560610 missense variant C/A;T snv 6
rs121908989
PRKAG2
0.882 0.080 7 151564199 missense variant T/A;C snv 4.0E-06 4
rs267606979
PRKAG2
0.882 0.080 7 151560560 missense variant A/G snv 3
rs779782995
HDAC9
0.925 0.040 7 18590438 missense variant A/G snv 1.7E-05 2
rs104894201
CRYAB
0.763 0.280 11 111908934 missense variant T/C snv 12
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 9
rs371401403
MYBPC3
0.807 0.080 11 47335996 missense variant G/A;T snv 6.8E-05; 7.9E-05 6
rs375882485
MYBPC3
0.827 0.080 11 47342698 missense variant G/A snv 4.0E-05 9.8E-05 5
rs397516005
MYBPC3
0.827 0.120 11 47333566 stop gained G/A snv 8.4E-06 2.8E-05 5
rs573916965
MYBPC3
0.827 0.080 11 47346297 stop gained C/A;T snv 2.5E-04 5
rs104894204
CSRP3
0.882 0.040 11 19188245 missense variant A/C snv 4
rs121917758
LRRC56 ; HRAS
0.851 0.160 11 533883 missense variant G/A snv 4
rs775404728
MYBPC3
0.851 0.080 11 47337535 missense variant G/A snv 4.0E-06 4
rs1352376969
MYBPC3
0.882 0.080 11 47341155 missense variant G/A;C snv 3
rs1412710023
MYBPC3
0.925 0.040 11 47343549 missense variant T/A snv 4.1E-06 3
rs397515985
MYBPC3
0.882 0.040 11 47335886 missense variant G/T snv 1.3E-04 2.0E-04 3
rs730880460
LRRC56 ; HRAS
0.882 0.120 11 533877 missense variant C/A;T snv 3
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 13
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 13
rs104894369
MYL2
0.807 0.080 12 110914287 missense variant C/A;T snv 10
rs35049558
MYL2
0.851 0.040 12 110914287 frameshift variant -/CT ins 8.0E-06 8
rs397507550
PTPN11
0.882 0.160 12 112489106 missense variant G/A;C snv 3