Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4665058
BAZ2B
2 159333698 intron variant A/C snv 0.90 2
rs12155623 8 48899642 regulatory region variant A/C;T snv 2
rs2077316
ZNF365
10 62465689 intron variant A/C;T snv 1
rs13022357
TANC1
2 159213245 intron variant A/G snv 0.83 2
rs16872085
ZFPM2
8 104945312 intron variant A/G snv 7.6E-02 2
rs17291650
ATF1
12 50819650 synonymous variant A/G snv 6.7E-02 6.4E-02 2
rs54211 22 39291479 upstream gene variant A/G snv 0.90 2
rs6716724 2 11370822 intergenic variant A/G snv 0.82 2
rs6730157
RAB3GAP1 ; ZRANB3
2 135149518 intron variant A/G snv 0.60 1
rs11624056 14 87039904 intergenic variant A/T snv 8.0E-02 2
rs2389202 4 116333133 intergenic variant A/T snv 0.78 2
rs1057518920
DSP
0.925 0.080 6 7575386 stop gained C/A snv 5
rs143978652
MYH6
0.882 0.080 14 23393437 missense variant C/A;T snv 9.3E-04; 4.0E-06 6
rs62641689
HCN4
15 73323818 missense variant C/A;T snv 3.2E-03 2
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 6
rs12189362
GRIA1
5 153677988 intron variant C/T snv 0.11 2
rs1559040
ACYP2
2 54120613 intron variant C/T snv 0.11 2
rs1823172 12 127308069 intergenic variant C/T snv 0.17 2
rs2281680
AP1G2 ; LOC102724814
14 23563861 splice region variant C/T snv 0.18 0.13 2
rs7307780
LOC105369844
12 75826838 intron variant C/T snv 0.18 2
rs2824292 0.925 0.080 21 17414857 regulatory region variant G/A snv 0.47 3
rs10183640
UPP2
2 157923692 intron variant G/A snv 0.31 2
rs16866933
ZNF385B ; LOC107985967
2 179701951 intron variant G/A snv 9.3E-02 2
rs4621553
LOC107986441
5 113694467 intergenic variant G/A snv 0.78 2
rs71352737
TRPM4
19 49182889 stop gained G/A snv 1.5E-03 1.6E-03 1