Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 4
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 3
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 3
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 2
rs12427353
HNF1A
1.000 0.080 12 120989098 intron variant G/A;C;T snv 2
rs2464196
HNF1A
0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 2
rs1183910
HNF1A
1.000 0.080 12 120983004 intron variant G/A snv 0.28 2
rs1169306
C12orf43 ; HNF1A
12 121000508 3 prime UTR variant C/T snv 0.31 1
rs7979473
HNF1A
12 120982457 intron variant A/C;G snv 1
rs7979478
HNF1A
12 120982460 intron variant A/C;G;T snv 1
rs2464195
HNF1A
12 120997672 missense variant G/A snv 0.39 0.31 1
rs11065385
HNF1A
12 120985583 intron variant A/G snv 0.72 1
rs1169286
HNF1A
1.000 0.080 12 120981253 intron variant T/C snv 0.39 1
rs1169303
HNF1A
12 120998573 intron variant A/C;G snv 0.45 1
rs2393775
HNF1A
12 120986771 intron variant G/A;C snv 1
rs2259820
HNF1A
0.882 0.160 12 120997539 synonymous variant C/T snv 0.34 0.26 1
rs1169300
HNF1A
0.882 0.080 12 120993422 intron variant G/A snv 0.27 1
rs1169302
HNF1A
12 120994499 intron variant T/A;G snv 0.40 1
rs735396
HNF1A ; C12orf43
12 121001041 3 prime UTR variant T/C snv 0.39 0.31 1
rs1800574
HNF1A ; HNF1A-AS1
0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02 1