Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199476301
TPM1
0.851 0.040 15 63042874 missense variant G/A;T snv 4.0E-06 6
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
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
rs121917776
VCL
0.882 0.040 10 74112086 missense variant C/T snv 9.9E-05 7.0E-06 5
rs535039125
CYP2B6
0.851 0.040 19 41004380 missense variant C/T snv 1.1E-04 1.3E-04 5
rs104894505
TPM1
0.882 0.040 15 63044072 missense variant G/A snv 4
rs111033559
PLN ; CEP85L
0.925 0.040 6 118558946 missense variant C/T snv 4
rs121909298
SGCD
0.925 0.040 5 156595000 missense variant T/G snv 2.0E-04 1.3E-04 4
rs139517732
TTN
0.851 0.040 2 178802273 missense variant C/T snv 4.4E-05 1.4E-05 4
rs1553265736
LMNA
0.925 0.040 1 156136080 missense variant G/C snv 4
rs1739843
HSPB7
0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs199476314
TPM1
0.882 0.040 15 63060930 missense variant T/G snv 4
rs2306969
LOC101928844 ; FUT3
0.925 0.040 19 5851790 intron variant A/G snv 0.76 4
rs267607158
TTN ; TTN-AS1
0.851 0.040 2 178740125 stop gained G/A snv 4
rs397516607
RBM20
0.925 0.040 10 110821356 missense variant G/A snv 4
rs397516695
DES
0.882 0.040 2 219418869 missense variant T/A;C snv 5.5E-05 4
rs61661343
LMNA
0.851 0.040 1 156130687 missense variant T/C snv 4
rs758264780
TPM1
0.882 0.040 15 63044029 frameshift variant G/- delins 4
rs10927875
ZBTB17
1.000 0.040 1 15972817 intron variant C/T snv 0.29 3
rs1212453165
TPM1
0.925 0.040 15 63043751 missense variant G/A snv 6.8E-06 3
rs138592977
LMNA
1.000 0.040 1 156135968 missense variant G/A snv 5.6E-05 6.3E-05 3
rs1393297693
SRF
1.000 0.040 6 43178806 missense variant G/A snv 4.0E-06 3
rs146275785
NEBL
0.925 0.040 10 20828531 missense variant G/A;T snv 7.2E-05; 2.7E-04 3
rs2234962
BAG3
1.000 0.040 10 119670121 missense variant T/C snv 0.17 0.15 3