Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7116456 11 23933767 intergenic variant T/C snv 0.97 2
rs4898521 12 49361379 downstream gene variant T/A snv 0.97 2
rs648425
PTGFR
1 78421523 intron variant T/C snv 0.95 2
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs7298909
SBNO1
12 123346392 intron variant C/T snv 0.89 2
rs1215112
TTC39B
9 15303585 intron variant G/A snv 0.89 2
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs2999159
MOV10
1 112688136 intron variant A/G snv 0.85 4
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs367070 19 54296648 upstream gene variant G/A snv 0.81 2
rs2763981
CYP21A2 ; SLC44A4
6 31872244 intron variant T/A snv 0.79 5
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs7118275
SOX6
11 16250132 intron variant C/T snv 0.78 2
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs670401
ARHGAP42
11 100701679 intron variant A/G snv 0.76 3
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 5
rs2749008
GSTA2
6 52761322 intron variant C/T snv 0.75 4
rs7791745 7 42345021 regulatory region variant T/C snv 0.73 2
rs10957054
UBXN2B
8 58423997 intron variant C/T snv 0.73 3
rs7096937
GPAM
10 112190660 intron variant T/C snv 0.72 5
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71 5
rs540730
R3HDM2
12 57413331 intron variant T/C snv 0.71 3
rs10734252 1.000 0.080 11 17383292 non coding transcript exon variant G/A snv 0.71 3
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs740746 10 114033028 intergenic variant G/A snv 0.70 8