Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6533183
TET2-AS1 ; TET2
4 105212027 intron variant C/T snv 0.61 3
rs670523
RIT1
1.000 0.040 1 155908941 intron variant A/G snv 0.48 3
rs7076938
LOC105378493
10 114029616 intergenic variant C/T snv 0.69 3
rs72656010
PLAG1 ; CHCHD7
8 56209656 intron variant T/C snv 0.10 3
rs798489
GNA12 ; AMZ1
7 2762169 splice donor variant C/T snv 0.20 3
rs9379832 1.000 0.080 6 26185972 downstream gene variant A/G snv 0.26 3
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 2
rs11055034
APOLD1 ; LOC107984129
1.000 0.080 12 12737692 intron variant C/A;T snv 2
rs11867479
KCNJ16
17 70094066 intron variant C/A;T snv 2
rs11893688
ADAM17
2 9555153 intron variant C/T snv 0.64 2
rs12153596
EBF1
5 158983170 non coding transcript exon variant C/T snv 0.30 2
rs12446550 16 28532060 downstream gene variant G/A snv 0.36 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
rs1482852
LINC02029
3 157080505 upstream gene variant A/G snv 0.46 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
rs2428362 17 7276955 upstream gene variant C/A;T snv 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
rs2908279 1.000 0.080 7 44135258 downstream gene variant T/G snv 0.59 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