Disease: Hemoglobin measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 9
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
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 5
rs11089823 22 37113139 upstream gene variant T/C snv 0.28 4
rs11089824 22 37113146 upstream gene variant A/C;T snv 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
rs5750373
MPST
22 37028990 non coding transcript exon variant G/A snv 0.49 4
rs763668 22 37115036 intergenic variant C/G;T snv 4