Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 10
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 8
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7