Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs567732903
BCHE
3 165838780 intron variant A/- delins 9.1E-05 1
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs1406961
NKAIN4
20 63264568 intron variant A/C snv 0.87 1
rs1440675 3 166153433 intergenic variant A/C snv 4.7E-02 1
rs1478011
LOC105374191
3 164554523 intergenic variant A/C snv 0.40 1
rs1545165 3 165915941 intergenic variant A/C snv 0.17 1
rs17706250 3 165657192 intron variant A/C snv 9.9E-02 1
rs1868530 3 165895121 intergenic variant A/C snv 8.1E-02 1
rs2024537 3 166169246 intergenic variant A/C snv 0.28 1
rs2024539 3 166167264 intergenic variant A/C snv 0.16 1
rs2668206
BCHE
3 165775666 intron variant A/C snv 0.51 1
rs4325882 3 166124518 intergenic variant A/C snv 0.62 1
rs4602440 3 165868486 intergenic variant A/C snv 0.87 1
rs656339 3 165621044 intron variant A/C snv 0.55 1
rs6776635 3 166140639 intergenic variant A/C snv 0.20 1
rs893522 3 165842830 intron variant A/C snv 0.11 1
rs9819444 3 165951393 intergenic variant A/C snv 0.16 1
rs9851453 3 166204028 intergenic variant A/C snv 0.48 1
rs9854178 3 166033739 intergenic variant A/C snv 0.41 1
rs9862986 3 166070594 intergenic variant A/C snv 0.35 1
rs9883928 3 166014220 intergenic variant A/C snv 0.37 1
rs10497870
NBEAL1
2 203105560 intron variant A/C;G snv 1
rs11921875 3 165718131 intron variant A/C;G snv 1
rs1947983
NBEAL1
2 203017870 intron variant A/C;G snv 1