HEMGN, hemogen, 55363

N. diseases: 26; N. variants: 3
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10984466
rs10984466 		9 97945710 upstream gene variant A/G snv 0.31
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs3758253
rs3758253 		9 97938372 intron variant C/T snv 0.30
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs755109
rs755109 		9 97933921 intron variant T/C snv 0.30
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		0.700 1.000 1 2009 2009
dbSNP: rs755109
rs755109 		9 97933921 intron variant T/C snv 0.30
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2009 2009