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
rs6090040
TCEA2
20 64060707 intron variant A/C snv 0.52 2
rs758801
STAB1
1.000 0.040 3 52502292 intron variant A/C snv 0.86 2
rs762705
LSMEM2 ; SEMA3B
3 50276096 non coding transcript exon variant A/C snv 2
rs10512606
RNF157
17 76215127 intron variant A/C snv 0.14 1
rs10843817
CAPRIN2
12 30712576 intron variant A/C snv 0.21 1
rs10844642 12 33577433 downstream gene variant A/C snv 0.27 1
rs11247113
MEF2A
15 99577110 intron variant A/C snv 0.44 1
rs11592754
EPC1
10 32330644 intron variant A/C snv 0.11 1
rs11726981
LOC105377406
4 124299553 intergenic variant A/C snv 0.30 1
rs13406302
CDC42EP3
2 37647707 intron variant A/C snv 0.36 1
rs144033177 20 590823 intergenic variant A/C snv 1.0E-02 1
rs1568799 7 42628277 intergenic variant A/C snv 0.31 1
rs270960 2 160858218 intergenic variant A/C snv 0.36 1
rs35915890
DGKB
7 14188819 intron variant A/C snv 0.30 1
rs39312
CFTR ; LOC105375467 ; WNT2
7 117314731 intron variant A/C snv 0.43 1
rs4536164
LGR4
11 27445562 intron variant A/C snv 0.70 1
rs4681011
ROBO1
3 78786588 intron variant A/C snv 0.61 1
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 1
rs62506196 8 59351906 intergenic variant A/C snv 0.21 1
rs6428789 1 119007857 regulatory region variant A/C snv 0.57 1
rs6727396
CCNT2-AS1
2 134741666 intron variant A/C snv 0.27 1
rs6795831 3 129622560 intergenic variant A/C snv 0.18 1
rs68162171
LOC102724064
11 66357990 intron variant A/C snv 0.23 1
rs7823561
LOC107986933
8 25784248 intergenic variant A/C snv 0.38 1