Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 5
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 5
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 5
rs12661667
USP49
6 41824807 intron variant C/T snv 0.20 4
rs13220662
HBS1L
6 135074410 intron variant G/A snv 0.41 4
rs1421312
TMPRSS6
22 37091770 intron variant A/G snv 0.45 4
rs1569534 6 135130442 intergenic variant C/T snv 0.21 4
rs17064262 6 135144336 intergenic variant T/C snv 0.18 4
rs198833 6 26114280 downstream gene variant G/A snv 0.87 4
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 4
rs2050019 6 135142809 intergenic variant C/T snv 0.27 4
rs218237 4 54528005 intergenic variant C/T snv 0.18 4
rs2274089
CARMIL1
6 25488355 intron variant C/T snv 5.9E-02 4
rs2856646
H2AC6
6 26135270 intron variant A/G snv 0.73 4
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 4
rs3806113
MED20
6 41908597 intron variant C/T snv 0.18 4
rs5756504
TMPRSS6
22 37071230 intron variant C/G;T snv 4
rs6569992 6 135131014 intergenic variant G/A;C;T snv 4
rs668459 6 139514552 intron variant C/T snv 0.51 4