Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs218237 4 54528005 intergenic variant C/T snv 0.18 5
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26 4
rs128494
CLDN14 ; LOC105369301
21 36461960 intron variant T/C snv 0.72 4
rs13335629
FAM234A
16 260381 intron variant G/A;C snv 1.1E-02 4
rs1936807
RSPO3
6 127127104 intron variant C/G snv 0.55 4
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 4
rs2968478 16 88792238 intergenic variant T/G snv 0.61 4
rs442177
AFF1
4 87109109 intron variant G/T snv 0.56 4
rs4791641
PFAS
17 8257831 missense variant C/T snv 0.43 0.41 4
rs6415788
GLIS3
9 4118111 missense variant G/T snv 0.67 0.62 4
rs837763
LOC107984842
16 88787321 upstream gene variant C/G;T snv 4
rs9399136
HBS1L
6 135081201 intron variant T/C snv 0.18 4
rs10168349
PRKCE
2 46133768 intron variant G/C snv 0.36 3