Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554218
NGEF
2 232894174 intron variant G/T snv 8.9E-02 1
rs6730157
RAB3GAP1 ; ZRANB3
2 135149518 intron variant A/G snv 0.60 1
rs71352737
TRPM4
19 49182889 stop gained G/A snv 1.5E-03 1.6E-03 1
rs2077316
ZNF365
10 62465689 intron variant A/C;T snv 1
rs10833905 11 23023046 regulatory region variant T/A snv 0.25 2
rs11624056 14 87039904 intergenic variant A/T snv 8.0E-02 2
rs12155623 8 48899642 regulatory region variant A/C;T snv 2
rs17718586 17 70648048 intergenic variant G/T snv 7.1E-02 2
rs1823172 12 127308069 intergenic variant C/T snv 0.17 2
rs2389202 4 116333133 intergenic variant A/T snv 0.78 2
rs54211 22 39291479 upstream gene variant A/G snv 0.90 2
rs6716724 2 11370822 intergenic variant A/G snv 0.82 2
rs6964415 7 46202985 intergenic variant T/A;C;G snv 2
rs1559040
ACYP2
2 54120613 intron variant C/T snv 0.11 2
rs2281680
AP1G2 ; LOC102724814
14 23563861 splice region variant C/T snv 0.18 0.13 2
rs10829156
ARL5B
10 18661626 intron variant T/C snv 0.79 2
rs17291650
ATF1
12 50819650 synonymous variant A/G snv 6.7E-02 6.4E-02 2
rs4665058
BAZ2B
2 159333698 intron variant A/C snv 0.90 2
rs2982694
ESR1
6 151964552 intron variant G/T snv 0.86 2
rs12189362
GRIA1
5 153677988 intron variant C/T snv 0.11 2
rs62641689
HCN4
15 73323818 missense variant C/A;T snv 3.2E-03 2
rs16942421
KCTD1
18 26576461 intron variant G/A;T snv 2
rs12429889
KLF12
13 74168185 intergenic variant T/C snv 0.29 2
rs7307780
LOC105369844
12 75826838 intron variant C/T snv 0.18 2
rs9581094
LOC105370117 ; TPTE2P6 ; PARP4
13 24508492 intron variant T/C snv 0.13 2