Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 11
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 7
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 6
rs2615061
LOC102723834
1 225708104 intron variant G/A snv 0.12 3
rs10489481 1 185422035 regulatory region variant G/A snv 0.31 2
rs115340020
RPAP2 ; GLMN
1 92300881 intron variant G/A snv 1.7E-02 2
rs11580646
TENT5C
1 117619797 intron variant C/G snv 0.14 2
rs12753280
EVI5
1 92550671 intron variant T/A;C snv 2
rs141094656
GLMN
1 92287779 intron variant T/C snv 1.3E-02 2
rs17608459
LINC01768
1 109892706 upstream gene variant G/A snv 7.9E-02 2
rs200895692
SLC2A1
1 42956286 intron variant GCCTGTAATCCCAG/- delins 2
rs35883536
LINC01349
1 100640978 non coding transcript exon variant G/A snv 0.46 2
rs4970966
ENSA
1 150611627 intron variant G/T snv 0.16 2
rs514406
ZYG11A
1 52864786 intron variant A/G;T snv 2
rs59072704
LOC105373262
1 244324625 intergenic variant T/C snv 0.23 2
rs6429432
LINC02768 ; LOC105373215
1 235943941 upstream gene variant A/C snv 0.93 2
rs67397717
CRYBG2
1 26327482 intron variant AAAAAAA/-;AAAA;AAAAA;AAAAAA;AAAAAAAA delins 2
rs708727
SLC41A1
1 205798757 synonymous variant G/A snv 0.30 0.29 2
rs72675573 1 56171209 intron variant C/T snv 0.27 2
rs7516138
PIK3CD
1 9651584 upstream gene variant A/G snv 0.52 2
rs1375493
ITGA4
2 181459039 non coding transcript exon variant G/A snv 0.56 3
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 3
rs10168795
DOCK10
2 224888625 intron variant A/G snv 0.24 2