Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894369
MYL2
0.807 0.080 12 110914287 missense variant C/A;T snv 10
rs1058402
PVR ; LOC107985305
0.925 0.040 19 44647342 missense variant G/A snv 7.7E-02 5.6E-02 3
rs113994099
POLG
0.827 0.240 15 89320883 missense variant T/C snv 10
rs117184249
SYNE1
1.000 0.120 6 152401278 missense variant C/T snv 9.3E-04 4.0E-04 3
rs118192170
RYR1
0.882 0.120 19 38584989 missense variant T/A;C snv 6
rs121434589
MYH2 ; MYHAS
0.851 0.200 17 10535137 missense variant C/T snv 8
rs121908211
CACNA1A
0.882 0.080 19 13371744 missense variant C/T snv 5
rs121908893
SLC22A5
1.000 0.160 5 132385435 stop gained C/A;T snv 5.3E-04; 1.2E-04 3
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 15
rs121913003
DES
0.882 0.200 2 219421532 missense variant C/T snv 6
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv 15
rs1356874787
PANK2 ; PANK2-AS1
20 3889103 start lost G/A snv 6.7E-06 2
rs1373219981
ATP13A2
1 17011736 start lost C/A snv 1.3E-05 2
rs1373863123
ACTB
1.000 0.080 7 5529540 missense variant G/A snv 4
rs137853305
TPM2
0.851 0.120 9 35685529 missense variant G/A snv 7
rs137853306
TPM2
0.882 0.080 9 35689265 missense variant C/T snv 6
rs1405183655
FA2H
16 74719132 missense variant C/G;T snv 4.0E-06 2
rs142000963
LMNA
0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs1805123
KCNH2
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06 18
rs199474714
TPM3
0.925 0.080 1 154173113 missense variant C/T snv 4
rs201573646
MAD2L1BP
6 43640526 missense variant G/A snv 1.0E-04 1.4E-05 2
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs28937581
DYSF
0.827 0.160 2 71570300 missense variant G/T snv 1.2E-05 9