Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 5
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs6020712
CTNNBL1
1.000 0.080 20 37758210 intron variant G/A snv 0.12 4
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 4
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 4
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 3
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 3
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 3
rs16986921
CTNNBL1
1.000 0.080 20 37754119 intron variant C/T snv 0.12 3
rs6013029
CTNNBL1
0.882 0.160 20 37771178 intron variant G/T snv 0.12 3
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 3
rs3744763
HNF1B
0.925 0.160 17 37730894 non coding transcript exon variant A/G snv 0.30 3
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 3
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 3