Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57414412 11 111898707 intergenic variant G/A snv 0.27 1
rs6033062 20 11226771 intergenic variant T/A;G snv 1
rs11680809 2 112813232 downstream gene variant C/A snv 0.55 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs2262207
DCUN1D2
13 113481795 intron variant A/G snv 0.39 1
rs73226528
USF3
3 113679795 intron variant T/C snv 0.15 1
rs7076938
LOC105378493
10 114029616 intergenic variant C/T snv 0.69 3
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs72760655
LOC105376225 ; COL27A1
9 114153934 upstream gene variant C/A;G snv 1
rs2574727
VGLL4
3 11595034 intron variant G/A snv 6.4E-02 1
rs6608539 X 116016501 intergenic variant G/A snv 1
rs1323438
PAPPA
9 116353252 intron variant T/A;C snv 1
rs636252 6 116836611 intergenic variant T/C snv 0.52 1
rs41276588
LOC100996263 ; TENT5C
1 117605762 non coding transcript exon variant G/A snv 0.21 1
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 4
rs80278614 1 118869694 intergenic variant G/A;T snv 1
rs10283100
ENPP2
8 119583783 missense variant A/G;T snv 0.96 3
rs2715026 4 119695650 downstream gene variant G/C snv 0.41 1
rs12623454 2 120568721 intergenic variant G/C;T snv 1
rs7847628
PHF19
9 120868947 intron variant A/C;G snv 2
rs3933326
PHF19
9 120871670 intron variant A/G snv 0.65 1
rs80019595
HNF1A ; HNF1A-AS1
12 120979503 intron variant C/G;T snv 1
rs139429176
LOC105370032
12 121194357 upstream gene variant C/T snv 6.8E-03 1
rs71486610
PLEKHA1
10 122375287 intron variant G/C snv 0.45 1
rs2421016
PLEKHA1
0.925 0.120 10 122407996 intron variant C/T snv 0.46 2