Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 6
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs35444 12 115114632 intergenic variant A/G snv 0.38 5
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 4
rs4722675
HOTTIP
7 27204343 intron variant A/G snv 0.93 4
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 4
rs6461992
HOXA10-HOXA9 ; HOXA11 ; HOXA10
1.000 0.120 7 27181212 3 prime UTR variant A/G snv 0.93 4
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs11067763
LOC105370003
12 115760536 intron variant A/G snv 0.16 3
rs11124945
PLEKHH2
1.000 0.040 2 43650017 intron variant A/G snv 0.21 3
rs1327235 20 10988382 intron variant A/G snv 0.46 3
rs16982520
ZNF831
1.000 0.040 20 59183665 intron variant A/G snv 0.14 3
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 3
rs6712094 2 164186950 intron variant A/G snv 0.23 3
rs6871087 0.925 0.040 5 30899410 intergenic variant A/G snv 8.5E-02 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs7651190
ULK4
1.000 0.160 3 41724463 intron variant A/G snv 0.33 3
rs820430 3 27507409 regulatory region variant A/G snv 0.30 3
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 3
rs9385284 6 123078960 intergenic variant A/G snv 0.24 3
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs17111503
PCSK9
0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 2
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 2