Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 2
rs10778215
C12orf42
12 103143488 intron variant T/A;G snv 2
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 2
rs3762220 20 18797336 upstream gene variant G/A;T snv 2
rs4817984 1.000 0.080 21 39093140 intergenic variant C/A;G snv 2
rs4910742
HBG2 ; HBE1
11 5285279 intron variant G/A;T snv 2
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 2
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 2
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 2
rs7160151 14 49336446 intergenic variant A/G;T snv 2
rs7979473
HNF1A
12 120982457 intron variant A/C;G snv 2
rs9378212 0.925 0.160 6 32477914 upstream gene variant C/G;T snv 2
rs10036128
LINC02196
5 6937069 intron variant G/A;C;T snv 1
rs10235512
RADIL
7 4865424 intron variant T/C;G snv 1
rs11108056 12 95461609 regulatory region variant C/G;T snv 1
rs1119582 5 125907327 intron variant T/C snv 1
rs11265191
OR10J1 ; OR10J4
1 159430569 intron variant C/G;T snv 1
rs11265263 1 159740727 intergenic variant C/A;T snv 1
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 1
rs1189402
LOC105370826
15 53435957 intron variant A/G;T snv 1
rs12023742 1 19965513 intergenic variant C/A;G snv 1
rs12202641
FRK
6 115993471 intron variant C/A;T snv 1
rs12427353
HNF1A
1.000 0.080 12 120989098 intron variant G/A;C;T snv 1
rs1292056
TUBD1
17 59881686 intron variant C/G;T snv 1
rs13375019 1 65657453 intergenic variant G/C;T snv 1