Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
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
rs104894201
CRYAB
0.763 0.280 11 111908934 missense variant T/C snv 12
rs104894369
MYL2
0.807 0.080 12 110914287 missense variant C/A;T snv 10
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 9
rs104894724
TNNI3
0.790 0.120 19 55154146 missense variant G/A;C snv 4.0E-06 8
rs121913627
MYH7
0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 8
rs121964856
TNNT2
0.807 0.120 1 201365297 missense variant C/A;T snv 8
rs35049558
MYL2
0.851 0.040 12 110914287 frameshift variant -/CT ins 8.0E-06 8
rs1057517686
ATAD3A
0.827 0.120 1 1529299 missense variant C/T snv 7
rs121913630
MYH7
0.851 0.080 14 23425814 missense variant G/A;C snv 1.2E-05 7
rs45586240
TNNT2
0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 7
rs104894502
TPM1
0.807 0.120 15 63060915 missense variant A/G;T snv 6
rs1057519819
MAP2K1
0.851 0.240 15 66436750 missense variant T/C snv 6
rs116840805
SSUH2 ; CAV3
0.827 0.160 3 8745725 missense variant C/T snv 6
rs121908991
PRKAG2
0.807 0.120 7 151560610 missense variant C/A;T snv 6
rs121964858
TNNT2
0.807 0.120 1 201365244 missense variant A/C;G;T snv 6
rs199476301
TPM1
0.851 0.040 15 63042874 missense variant G/A;T snv 4.0E-06 6
rs267607124
TNNC1
0.807 0.080 3 52451410 missense variant G/A;C;T snv 4.0E-05; 4.0E-06; 1.3E-04 6
rs371401403
MYBPC3
0.807 0.080 11 47335996 missense variant G/A;T snv 6.8E-05; 7.9E-05 6
rs104894729
TNNI3
0.827 0.080 19 55151892 missense variant C/A;G;T snv 5
rs36211715
MYH7
0.851 0.080 14 23424839 missense variant C/A;G;T snv 4.0E-06 5