Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10183640
UPP2
2 157923692 intron variant G/A snv 0.31 2
rs1057518920
DSP
0.925 0.080 6 7575386 stop gained C/A snv 5
rs10765792
MAML2
11 96133536 intron variant G/C snv 0.10 2
rs10829156
ARL5B
10 18661626 intron variant T/C snv 0.79 2
rs10833905 11 23023046 regulatory region variant T/A snv 0.25 2
rs111033560
PLN ; CEP85L
0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs11187837
PLCE1
10 94276223 intron variant T/C snv 8.4E-02 2
rs11624056 14 87039904 intergenic variant A/T snv 8.0E-02 2
rs12155623 8 48899642 regulatory region variant A/C;T snv 2
rs12189362
GRIA1
5 153677988 intron variant C/T snv 0.11 2
rs12429889
KLF12
13 74168185 intergenic variant T/C snv 0.29 2
rs13022357
TANC1
2 159213245 intron variant A/G snv 0.83 2
rs143978652
MYH6
0.882 0.080 14 23393437 missense variant C/A;T snv 9.3E-04; 4.0E-06 6
rs1554218
NGEF
2 232894174 intron variant G/T snv 8.9E-02 1
rs1559040
ACYP2
2 54120613 intron variant C/T snv 0.11 2
rs16866933
ZNF385B ; LOC107985967
2 179701951 intron variant G/A snv 9.3E-02 2
rs16872085
ZFPM2
8 104945312 intron variant A/G snv 7.6E-02 2
rs16942421
KCTD1
18 26576461 intron variant G/A;T snv 2
rs17291650
ATF1
12 50819650 synonymous variant A/G snv 6.7E-02 6.4E-02 2
rs17718586 17 70648048 intergenic variant G/T snv 7.1E-02 2
rs1823172 12 127308069 intergenic variant C/T snv 0.17 2
rs2077316
ZNF365
10 62465689 intron variant A/C;T snv 1
rs2251393
MARCHF10
1.000 0.080 17 62701571 3 prime UTR variant G/A;C snv 0.85; 4.9E-05 3
rs2281680
AP1G2 ; LOC102724814
14 23563861 splice region variant C/T snv 0.18 0.13 2
rs2389202 4 116333133 intergenic variant A/T snv 0.78 2