Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11078903
CDK12
17 39475671 intron variant G/A;C;T snv 2
rs9944411
FBXL20
17 39327346 intron variant T/C snv 0.32 2
rs10068737 5 118700852 intergenic variant T/A;C snv 1
rs1009840
SGK1 ; LOC107986646
6 134225547 intron variant G/A snv 0.53 1
rs1168357
GRIP1
12 66356099 intron variant T/C snv 0.50 1
rs12124078
DNAJC16
1 15543404 intron variant A/G snv 0.32 1
rs12575381 11 135033566 regulatory region variant G/A snv 0.16 1
rs1500896
C8orf37-AS1
8 95474454 intron variant G/A;C snv 1
rs2453580
SLC47A1
17 19535008 non coding transcript exon variant T/C snv 0.37 1
rs2880072 6 159404417 downstream gene variant G/A snv 0.49 1
rs2887915 2 210689850 intergenic variant C/G;T snv 1
rs2928148
INO80
15 41109352 intron variant G/A snv 0.44 1
rs3093058
CRP
1 159715525 upstream gene variant T/A;C;G snv 1
rs316029
SLC22A2
6 160265636 intron variant T/C snv 0.89 1
rs4555246
DOK6
18 69609486 intron variant G/A;T snv 1
rs500456 7 54531089 intergenic variant A/G snv 0.47 1
rs571461077
DOK6
18 69609487 intron variant ATAAATAA/-;ATAA;ATAAATAAATAA;ATAAATAAATAAATAA;ATAAATAAATAAATAAATAA;ATAAATAAATAAATAAATAAATAA delins 1
rs58206678
DOK6
18 69609487 intron variant ATAAATAA/-;ATAA;ATAAATAAATAA;ATAAATAAATAAATAA;ATAAATAAATAAATAAATAA;ATAAATAAATAAATAAATAAATAA delins 1
rs6428106
LOC105371664
1 192585301 intron variant G/T snv 0.14 1
rs6546837
ALMS1
2 73450771 missense variant G/C;T snv 0.27 1
rs6581768
LOC105369816
12 67683408 intergenic variant A/G snv 0.25 1
rs6865647
PDE4D
5 59103374 intron variant A/G;T snv 1
rs7784820
CD36
7 80420717 intron variant A/G snv 0.16 1
rs12922822
UMOD
1.000 0.040 16 20356323 upstream gene variant C/A;T snv 1
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 4