Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs10923724 1 119004219 upstream gene variant C/T snv 0.53 3
rs10927263
NID1
1 236017804 intron variant A/G snv 0.30 1
rs10933
GNL3 ; PBRM1
3 52685800 5 prime UTR variant C/T snv 0.39 1
rs10963067
CNTLN
9 17367948 intron variant C/A;T snv 1
rs10980797
LOC105376219
9 111150273 intron variant A/G;T snv 3
rs10980802
LOC105376219
9 111156576 intron variant A/G snv 0.37 1
rs10988105
ZDHHC12
9 128722247 intron variant C/T snv 0.39 1
rs10991433 9 104964637 intergenic variant T/C snv 8.2E-02 1
rs10992396
LOC107987095
9 92674850 upstream gene variant A/G snv 0.17 1
rs10992408 9 92682518 intergenic variant A/G snv 0.20 1
rs10993017 9 93998102 intergenic variant T/A;C snv 0.31 1
rs11016883
MGMT
10 129702676 intron variant G/C snv 0.38 1
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72 1
rs11042841
AMPD3
11 10483662 intron variant C/G snv 0.70 1
rs11048470
LOC107984482
12 26334350 intron variant G/T snv 0.26 1
rs11051005
IPO8
12 30630541 3 prime UTR variant A/G snv 0.18 1
rs11051048
CAPRIN2
12 30742783 intron variant G/A snv 0.21 1
rs11055887 12 14264245 intergenic variant G/A snv 0.14 1
rs11057450
ZNF664-RFLNA ; RFLNA
12 124100790 intron variant G/A snv 0.28 1
rs11057553
ZNF664-RFLNA ; RFLNA
12 124267534 intron variant C/T snv 3.9E-02 1
rs1105881
MAPKBP1
15 41780332 intron variant C/G snv 0.29 1
rs11059476 12 122708052 intron variant C/T snv 3.9E-02 1
rs11060344
HIP1R
12 122844554 intron variant A/G snv 9.5E-02 1