Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6993442 8 129683891 upstream gene variant G/C snv 0.17 5
rs11327184
CCDC26
8 129592027 intron variant C/- delins 0.40 4
rs13138355 4 82624823 upstream gene variant C/A;T snv 4
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53 4
rs413141 19 6675978 downstream gene variant A/G snv 0.84 4
rs4432538
PLCB1 ; LOC105372521
20 8626746 intron variant G/A snv 0.52 4
rs45577137
CEBPD
8 47739071 upstream gene variant A/G;T snv 4
rs72699818
RIN3
14 92611266 intron variant T/C snv 0.12 4
rs7288670
GGT5
22 24225858 intron variant A/C;G snv 4
rs10418046
NLRP12
19 53824615 upstream gene variant T/G snv 0.26 3
rs10980797
LOC105376219
9 111150273 intron variant A/G;T snv 3
rs113760175
CASC15
6 22343363 intron variant G/A;T snv 3
rs1157008 9 88920798 regulatory region variant T/C;G snv 3
rs11611647 12 4224753 intergenic variant T/C snv 0.22 3
rs11642657 16 85982722 intron variant C/A;T snv 3
rs12151289 19 33260946 intergenic variant G/A;C;T snv 3
rs12459847
MARK4
19 45247899 intron variant G/C snv 0.19 3
rs1375493
ITGA4
2 181459039 non coding transcript exon variant G/A snv 0.56 3
rs1991866
CCDC26
8 129611859 intron variant G/A;C snv 3
rs2238783
ARVCF
22 19984929 intron variant C/G snv 0.42 3
rs2615061
LOC102723834
1 225708104 intron variant G/A snv 0.12 3
rs28722705
ANKRD55
5 56158115 intron variant A/T snv 9.9E-02 3
rs45474992
BBC3
19 47221307 3 prime UTR variant C/T snv 2.4E-02 3
rs475616 10 30207976 regulatory region variant A/G snv 0.67 3
rs4807440
CNN2
19 1026478 upstream gene variant G/T snv 0.65 3