Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1936797 6 127111512 intron variant A/G snv 0.33 3
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 3
rs4465830
ZNF335
20 45956781 intron variant A/G snv 0.13 3
rs4703642
LOC105379040
5 74966337 intron variant A/G snv 0.50 3
rs1880241
STEAP1B
7 22719850 intron variant A/G snv 0.51 2
rs1998303 9 82800066 intergenic variant A/G snv 0.37 2
rs2686555
CABP1
12 120657369 intron variant A/G snv 0.52 2
rs34471628
DUSP1
5 172769749 missense variant A/G snv 2.4E-02 2.2E-02 2
rs4841133
LOC157273
8 9326154 non coding transcript exon variant A/G snv 0.87 2
rs771767 1.000 0.080 3 102029794 regulatory region variant A/G snv 0.70 2
rs814295
GCKR
0.925 0.120 2 27520348 intron variant A/G snv 0.18 2
rs10745954
C12orf42
12 103089316 intron variant A/G snv 0.60 1
rs11265260 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 1
rs117246187
RIPOR3
20 50690397 intron variant A/G snv 5.7E-02 1
rs12034598
CR1
1 207584170 intron variant A/G snv 0.19 1
rs12083537
IL6R
0.882 0.200 1 154408627 intron variant A/G snv 0.22 1
rs12568139 1 19985183 upstream gene variant A/G snv 6.0E-02 1
rs1514895 3 170987904 intron variant A/G snv 0.37 1
rs17401735
OTUD3
1 19910238 3 prime UTR variant A/G snv 0.21 1
rs2233688
PLA2G2E
1 19924237 upstream gene variant A/G snv 0.16 1
rs2239222
RGS6
14 72545177 intron variant A/G snv 0.43 1
rs2246469 1 159721022 intergenic variant A/G snv 0.58 1
rs2526932
RGS6
14 72614360 downstream gene variant A/G snv 0.65 1
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 1
rs4092465 18 57413205 intergenic variant A/G snv 0.46 1