Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11605518 11 13248667 intergenic variant A/G snv 0.72 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs3937593
LOC105374843
2 85983150 intergenic variant C/T snv 0.71 1
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 3
rs7685862
ENPEP
4 110467945 intron variant C/A snv 0.68 1
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs2246490 14 103517957 downstream gene variant G/T snv 0.67 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs1801020
GRK6 ; F12 ; SLC34A1
1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 4
rs1800389
WRN
8 31067041 synonymous variant C/T snv 0.71 0.67 1
rs6536076
LOC105377505
4 155499453 intron variant A/T snv 0.66 2
rs1155311
DLG2
11 83778372 intron variant A/T snv 0.66 1
rs35134
ERAP1
5 96823820 intron variant A/G snv 0.65 1
rs2943652 2 226243730 intergenic variant C/T snv 0.65 2
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 5
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 1
rs7694531
UNC5C
4 95165950 3 prime UTR variant A/G snv 0.64 2
rs6800730 3 48132720 intergenic variant A/G snv 0.64 1
rs4948550
BICC1
10 58828793 missense variant T/C snv 0.71 0.64 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1074703
NCALD
8 101803258 intron variant C/A snv 0.63 1
rs4277405 17 63471557 upstream gene variant C/T snv 0.63 4
rs11048457
LOC105369705
12 26310241 intron variant G/A snv 0.62 1