Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1009977
LGALS3
1.000 0.040 14 55136284 intron variant T/G snv 0.48 2
rs104893823
TNNC1
0.882 0.040 3 52451285 missense variant C/T snv 5
rs104894501
TPM1
0.851 0.040 15 63044030 stop gained G/A;C;T snv 4.0E-06 5
rs104894505
TPM1
0.882 0.040 15 63044072 missense variant G/A snv 4
rs1057515421
LMNA
0.925 0.120 1 156136284 stop gained C/T snv 2
rs1071646
TPM1
1.000 0.040 15 63059641 splice region variant C/A snv 0.67 0.65 1
rs10880
LTBP4
0.925 0.160 19 40622404 missense variant C/T snv 0.38 0.39 2
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10927875
ZBTB17
1.000 0.040 1 15972817 intron variant C/T snv 0.29 3
rs111033559
PLN ; CEP85L
0.925 0.040 6 118558946 missense variant C/T snv 4
rs11465817
IL23R
0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs11570113
MYBPC3
1.000 0.040 11 47333605 missense variant G/A;T snv 1.2E-05 1
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1165819867
LMNA
1.000 0.040 1 156134892 missense variant G/A;T snv 1
rs1175271580
LMOD2
1.000 0.040 7 123662780 stop gained G/A;T snv 1
rs118204016
MIR324 ; ACADVL
0.925 0.240 17 7223984 missense variant G/A snv 2.4E-05 1.4E-05 4
rs1212453165
TPM1
0.925 0.040 15 63043751 missense variant G/A snv 6.8E-06 3
rs121434420
PKP2
0.851 0.120 12 32879021 stop gained G/A snv 4.0E-06 4.9E-05 5
rs121909298
SGCD
0.925 0.040 5 156595000 missense variant T/G snv 2.0E-04 1.3E-04 4
rs121913002
DES
0.851 0.160 2 219425727 missense variant C/A;G;T snv 6.5E-05; 5.6E-04 7
rs121917776
VCL
0.882 0.040 10 74112086 missense variant C/T snv 9.9E-05 7.0E-06 5
rs1241664568
PRDX5
1.000 0.040 11 64320661 missense variant A/G snv 1.4E-05 1
rs1266360671
RYR2
0.925 0.080 1 237270518 missense variant T/C snv 4.7E-06 3
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100