Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5914101
FAAH2
X 57413512 intron variant G/A snv 0.33 1
rs762080
IGSF1 ; LOC102723546 ; LOC107985705
X 131400056 intron variant C/A;T snv 1
rs11703376 22 49282787 intergenic variant C/T snv 0.20 1
rs12167144
EIF4HP2 ; OSBP2 ; LOC107985544
22 30902221 non coding transcript exon variant A/C snv 0.36 1
rs13053505 22 38849613 intergenic variant G/A;C;T snv 1
rs5756052 22 21914386 intergenic variant A/G snv 0.43 1
rs6009583 22 49281720 intergenic variant C/A;T snv 1
rs9616551 22 49284503 intergenic variant A/C;G snv 1
rs2836950
BRWD1
21 39232503 splice region variant C/A;G snv 9.0E-06; 0.37 1
rs35184820
LINC00649
21 33948637 intron variant T/G snv 0.45 1
rs4818008
BRWD1
21 39239516 intron variant T/A snv 0.34 1
rs73204208
CHAF1B
21 36419168 downstream gene variant T/G snv 0.10 1
rs6087709 20 35430145 upstream gene variant C/G snv 0.25 2
rs2425670
YWHAB
20 44893088 intron variant G/A snv 0.61 1
rs35255016 20 38666096 regulatory region variant C/T snv 0.17 1
rs3746619
MC3R
0.925 0.200 20 56248749 5 prime UTR variant C/A snv 0.14 0.21 1
rs3828002
SLC24A3
20 19721405 3 prime UTR variant G/A;T snv 1
rs6010651
ZBTB46
20 63786890 intron variant A/C snv 0.43 1
rs6039251
PLCB1
20 8748849 intron variant T/C snv 0.34 1
rs6045400
DZANK1
20 18441344 intron variant A/G snv 0.72 1
rs6046818 20 20365534 non coding transcript exon variant T/C snv 0.22 1
rs6066454
SULF2
20 47735538 intron variant C/T snv 0.28 1
rs6136033
PCSK2 ; LOC105372546
20 17227859 intron variant A/C snv 0.56 1
rs7273470
GGT7
20 34869118 intron variant G/C snv 0.22 1
rs73898513
MACROD2
20 15825565 intron variant C/G;T snv 1