Disease: Cardiomyopathies
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
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
rs104894724
TNNI3
0.790 0.120 19 55154146 missense variant G/A;C 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
rs45586240
TNNT2
0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 7
rs199476301
TPM1
0.851 0.040 15 63042874 missense variant G/A;T snv 4.0E-06 6
rs104894204
CSRP3
0.882 0.040 11 19188245 missense variant A/C snv 4
rs121908989
PRKAG2
0.882 0.080 7 151564199 missense variant T/A;C snv 4.0E-06 4
rs267607123
TNNC1
0.882 0.080 3 52452222 missense variant A/T snv 4.0E-06 7.0E-06 4
rs1412710023
MYBPC3
0.925 0.040 11 47343549 missense variant T/A snv 4.1E-06 3