Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11615755
MED21
12 27063628 intron variant T/G snv 0.35 1
rs11643209
CFDP1
16 75297146 intron variant T/G snv 3.8E-02 1
rs12675715
TSNARE1
8 142270206 intron variant T/G snv 0.58 1
rs13020428 2 113675066 downstream gene variant T/G snv 0.13 1
rs1449386
CADM2
3 85569929 intron variant T/G snv 0.54 1
rs147202915 5 115058718 intergenic variant T/G snv 0.54 1
rs17035181 4 156757359 downstream gene variant T/G snv 0.16 1
rs17114641
SUFU
10 102527602 intron variant T/G snv 9.4E-02 1
rs1729413 2 200221940 intergenic variant T/G snv 0.49 1
rs1860509
TBXAS1 ; HIPK2
7 139778376 5 prime UTR variant T/G snv 0.37 1
rs246978 5 68710219 regulatory region variant T/G snv 0.25 1
rs28866311 15 41149997 regulatory region variant T/G snv 0.50 1
rs35320172
RBPMS
8 30442232 intron variant T/G snv 0.17 1
rs35450617
RBFOX1
16 6839674 intron variant T/G snv 0.39 1
rs3785880
MAPT
1.000 0.040 17 45916010 intron variant T/G snv 0.40 1
rs55678414
DOT1L
19 2177626 intron variant T/G snv 0.17 1
rs61918270
AEBP2
12 19677397 intron variant T/G snv 3.6E-02 1
rs6540125
BANP
16 87960283 intron variant T/G snv 0.68 1
rs6987335
SLC45A4
8 141225259 non coding transcript exon variant T/G snv 0.33 1
rs7042283
PIP5K1B
9 68903111 intron variant T/G snv 0.15 1
rs72834453
HTRA1
10 122475710 intron variant T/G snv 0.11 1
rs73169175
TCF20
22 42325368 intron variant T/G snv 8.2E-02 1
rs863930 3 136230895 intergenic variant T/G snv 0.52 1
rs9965695
LOC107984031
18 49735244 downstream gene variant T/G snv 6.5E-03 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25