Disease: Corpuscular Hemoglobin Concentration Mean
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 5
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs9402686
LOC105378010
6 135106679 upstream gene variant G/A snv 0.20 4
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 3
rs5756506
TMPRSS6
22 37071352 intron variant G/A;C snv 3
rs9609565 22 32471541 upstream gene variant G/A snv 0.24 2