Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11434755 11 18045473 upstream gene variant -/A delins 0.41 1
rs562306828 20 45928576 non coding transcript exon variant -/G;GAG;GAGAG ins 1
rs151105710
STAG1
3 136406836 intron variant -/GAATTAAA delins 0.16 1
rs3832016
CELSR2
1 109275536 3 prime UTR variant -/T ins 0.74 1
rs34696509
UVRAG
11 75841535 intron variant A/-;AA delins 0.18 1
rs34879232
SARM1 ; SLC46A1
17 28395021 3 prime UTR variant A/-;AA;AAA delins 1
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 5
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 3
rs4805881
PEPD
19 33405526 intron variant A/C snv 0.69 3
rs11078917 17 39590106 intergenic variant A/C snv 0.56 2
rs146524044
MYO5B
18 50057046 intron variant A/C snv 1.0E-03 2
rs7519429
DNM3 ; PIGC
1 172380106 intron variant A/C snv 0.29 2
rs10091038 8 29502788 intergenic variant A/C snv 0.57 1
rs111439884
RBM6
3 49986605 intron variant A/C snv 0.47 1
rs1117816
TMPRSS11E
4 68483300 intron variant A/C snv 0.19 1
rs13076253
CPNE4
3 132032931 intron variant A/C snv 0.15 1
rs192489212
CEP164
11 117349713 intron variant A/C snv 9.4E-04 1
rs7121538
COPB1
11 14482917 intron variant A/C snv 0.17 1
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 1
rs76213020
GNG2
14 51969287 3 prime UTR variant A/C snv 4.2E-03 1
rs7849420
MIR31HG
9 21499625 intron variant A/C snv 0.65 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs77960347
LIPG
18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 5