rs62160676, MIR4435-2HG

N. diseases: 5
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
1206 2 111410354 intron variant T/C;G snv 0.700 1.000 2 2016 2019
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 2 111410354 intron variant T/C;G snv 0.700 1.000 2 2016 2019
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 2 111410354 intron variant T/C;G snv 0.700 1.000 1 2016 2016
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 2 111410354 intron variant T/C;G snv 0.700 1.000 1 2016 2016
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 2 111410354 intron variant T/C;G snv 0.700 1.000 1 2016 2016