Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 1
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 2
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 2
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 2
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 3
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 1
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 1
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 1
rs1339552
BNC2
1.000 0.120 9 16848792 intron variant C/T snv 0.52 1
rs4961501
BNC2
1.000 0.120 9 16851680 intron variant T/A;C;G snv 1
rs12379687
BNC2
1.000 0.120 9 16854369 intron variant G/A;T snv 1
rs1416742
BNC2
1.000 0.120 9 16856885 intron variant G/A snv 0.43 1
rs10756819
BNC2
1.000 0.120 9 16858086 intron variant G/A;C;T snv 1
rs7861573
BNC2
1.000 0.120 9 16862282 intron variant A/G;T snv 1
rs2153271
BNC2
0.925 0.160 9 16864523 intron variant C/T snv 0.43 2
rs367899983
BNC2
1.000 0.120 9 16864524 intron variant GTCT/- delins 4.2E-05 2
rs12379183
BNC2
1.000 0.120 9 16865701 intron variant A/G snv 0.26 1
rs10962656 1.000 0.120 9 16877790 intergenic variant G/A snv 0.10 1
rs10810666 1.000 0.120 9 16911668 intergenic variant C/T snv 0.14 1
rs4445329 1.000 0.120 9 16911759 intergenic variant G/A;C snv 1
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 3