Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 6
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 4
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 4
rs2523578 1.000 6 31360765 upstream gene variant G/A snv 0.79 4
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs3748069
ADGRG6
6 142446496 downstream gene variant A/G snv 0.39 3
rs4896582
ADGRG6
6 142382740 intron variant G/A snv 0.50 3
rs6959212 7 38088724 intergenic variant T/C;G snv 3
rs7763064 6 142476152 intergenic variant G/A snv 0.38 3
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 2
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57 2
rs1659127 16 14294448 intergenic variant G/A;C;T snv 2
rs1991431
ZBTB38
3 141414608 intron variant G/A snv 0.50 2
rs263179
LOC153910
6 142542751 intron variant T/C snv 0.38 2
rs314268
LIN28B
6 104970103 intron variant G/A snv 0.64 2
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 2
rs4549631 6 126645162 intron variant T/C;G snv 2
rs6058227
UQCC1
20 35308144 intron variant C/T snv 0.15 2
rs6937121
ADGRG6
6 142385996 intron variant T/G snv 0.47 2
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 2
rs7753012
ADGRG6
6 142424746 intron variant T/G snv 0.50 2
rs7846385 8 77247943 intergenic variant T/C snv 0.23 2
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 2
rs9391253
LIN28B-AS1
6 104919741 intron variant A/T snv 0.29 2