Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 2
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 2
rs1000668
TMC1
9 72790943 intron variant T/A;G snv 1
rs10274928
JAZF1
7 28102469 intron variant A/G;T snv 1
rs10454127
FLACC1
2 201347651 intron variant G/A;T snv 1
rs1323135
SDCBP2-AS1 ; FKBP1A ; FKBP1A-SDCBP2
20 1377208 non coding transcript exon variant G/C;T snv 1
rs2409764
FAM167A ; FAM167A-AS1
8 11423764 3 prime UTR variant A/G;T snv 1
rs26704
PDE4D
5 59237827 intron variant A/G;T snv 1
rs4148641
ABCC8
11 17399926 intron variant G/A;T snv 1
rs6435079
FLACC1
2 201335608 intron variant C/G;T snv 1
rs6503659 1.000 0.040 17 41741012 intergenic variant A/C;G;T snv 1
rs753724
PLCE1
0.882 0.080 10 94291660 intron variant G/A;C;T snv 1
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 3
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs16901549
PCAT1 ; LOC105375751
8 126583939 intron variant G/T snv 8.6E-03 1
rs3805322
ADH4 ; LOC100507053
1.000 0.080 4 99135847 intron variant A/G snv 1.1E-02 1
rs6140125
SLC52A3
20 764903 intron variant C/A snv 1.5E-02 1
rs11065783
LOC105369980 ; LINC01405
12 110958445 non coding transcript exon variant A/G snv 1.9E-02 1
rs6772209 1.000 0.080 3 175929377 intergenic variant G/A snv 4.1E-02 1
rs8030672 1.000 0.080 15 68766745 intergenic variant T/A snv 5.4E-02 1