rs11966072, CCDC162P

N. diseases: 4
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 6 109313625 intron variant A/G snv 0.26 0.700 1.000 1 2010 2010
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 6 109313625 intron variant A/G snv 0.26 0.700 1.000 1 2010 2010
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 6 109313625 intron variant A/G snv 0.26 0.700 1.000 1 2010 2010
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 6 109313625 intron variant A/G snv 0.26 0.700 1.000 1 2010 2010