Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 15
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 7
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 5
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 4
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 4
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 4
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25 4
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 4
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 3
rs13322435 3 157077679 upstream gene variant A/G snv 0.46 3
rs1818782
DAB2 ; C9
5 39424526 intron variant A/C snv 0.56 3
rs2168101
LMO1 ; LOC105376536
0.827 0.200 11 8233861 intron variant C/A snv 0.24 3
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs2292626
PLEKHA1
0.925 0.120 10 122427198 intron variant C/T snv 0.46 3
rs2928148
INO80
15 41109352 intron variant G/A snv 0.44 3
rs34776209 7 23473474 upstream gene variant C/T snv 0.18 3
rs35261542
CDKAL1
1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 3