rs11338569, ANP32B

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 9 98001175 intron variant T/-;TT delins 0.25 0.700 1.000 1 2016 2016
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 9 98001175 intron variant T/-;TT delins 0.25 0.700 1.000 1 2016 2016