Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9399136
HBS1L
6 135081201 intron variant T/C snv 0.18 4
rs10168349
PRKCE
2 46133768 intron variant G/C snv 0.36 3
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 3
rs114948639
PRKCE
2 46066687 intron variant C/T snv 7.2E-03 3
rs115986297
GMDS
6 2050557 intron variant A/C;G snv 3
rs11689538
TFCP2L1
2 121238062 intron variant G/C snv 0.11 3
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 3
rs12811512
GPRC5A
12 12893277 intron variant C/T snv 0.11 3
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 3
rs17773190
LINC01118
2 46803224 intron variant A/G snv 0.32 3
rs1997595 21 15205839 intron variant A/C;G snv 3
rs2000999
HPR ; TXNL4B
1.000 0.080 16 72074194 intron variant G/A snv 0.16 3
rs2236496
RCL1
9 4844265 intron variant T/C snv 0.19 3
rs2269188
SIM2 ; LOC107985492 ; LOC105369308
21 36700056 intron variant G/C snv 0.24 3
rs2279434
MARCHF8
10 45459616 intron variant C/T snv 7.1E-02 3
rs366684
PROX1
1 214013919 intron variant G/A;C snv 3
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 3
rs531909210
TFR2
7 100641799 intron variant G/A snv 2.8E-03 3
rs533281866
EGLN1
1 231422308 intron variant G/A;C snv 3
rs56262900
KLHL29
2 23674855 intron variant G/A snv 7.6E-02 3
rs563995
KCNN4
19 43774629 intron variant G/A snv 0.24 0.34 3
rs5758896
A4GALT
22 42719570 intron variant T/C snv 0.55 3
rs5762813
ZNRF3
22 28807326 intron variant C/T snv 0.25 3
rs57908212
AP3D1
19 2161322 intron variant T/C snv 0.46 3
rs632057 6 139512875 intron variant T/G snv 0.57 3