Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11893688
ADAM17
2 9555153 intron variant C/T snv 0.64 2
rs12656216
SKP2
5 36160566 intron variant G/A snv 0.64 2
rs12909648
AKAP13
15 85681339 intron variant G/A snv 0.40 2
rs1415701
L3MBTL3
6 130024690 intron variant G/A snv 0.31 2
rs2131354
HHIP
4 144678756 intron variant G/A snv 0.41 2
rs2421016
PLEKHA1
0.925 0.120 10 122407996 intron variant C/T snv 0.46 2
rs2608029
PVT1
1.000 0.040 8 128157880 intron variant C/G snv 0.37 2
rs28530618 20 32687779 intron variant A/C;G snv 2
rs339969
RORA ; RORA-AS1
15 60591082 intron variant C/A snv 0.68 2
rs4932373
FES
1.000 0.040 15 90886057 intron variant A/C snv 0.25 2
rs6569647
L3MBTL3
6 130016121 intron variant T/C snv 0.34 2
rs6845999
HHIP ; HHIP-AS1
4 144644674 intron variant C/T snv 0.35 2
rs6925689 6 126544738 intron variant T/C snv 0.45 2
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 2
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 2
rs7541039
PROX1
1 214003436 intron variant C/T snv 0.27 2
rs7780752
GNGT1
7 93612328 intron variant T/C snv 0.27 2
rs7847628
PHF19
9 120868947 intron variant A/C;G snv 2
rs925098
LCORL
4 17918188 intron variant G/A snv 0.70 2
rs9267812
PPT2 ; PPT2-EGFL8
6 32160617 intron variant C/G;T snv 2
rs10147938
HEATR5A
14 31416745 intron variant C/T snv 0.32 1
rs10402712
PEPD
19 33435107 intron variant G/A snv 0.30 1
rs10509669
PLCE1
10 94210156 intron variant A/T snv 0.22 1
rs10734564
PTPRJ
11 48138877 intron variant A/G snv 0.74 1
rs10872678
ESR1
6 151718829 intron variant T/C snv 0.33 1