Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 4
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 3
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 3
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs10518693
IVD
15 40407823 intron variant C/T snv 0.37 2
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs11185790
PANK1
10 89612776 intron variant G/A snv 0.15 2
rs12670403
LOC101927609 ; AHR
7 17269655 intron variant C/A snv 0.46 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 2
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 2
rs1447352 11 92989595 downstream gene variant G/A snv 0.55 2
rs1495743 8 18415790 intergenic variant G/A;C snv 2
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2
rs2216405 2 210752170 intergenic variant A/G snv 0.15 2
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs2518049
AKR1C3
10 5095844 intron variant A/G;T snv 2
rs2624265
LINC02694
15 38856448 intron variant T/C snv 0.28 2
rs2652822
LACTB ; RPS27L
15 63130573 3 prime UTR variant T/C snv 0.41 2
rs272889
SLC22A4 ; MIR3936HG
5 132329685 intron variant A/G snv 0.64 2