Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16926246
rs16926246
HK1
10 69333636 intron variant C/T snv 0.12
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.800 1.000 2 2009 2017
dbSNP: rs10159477
rs10159477
HK1
10 69340132 intron variant G/A snv 0.14
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17476364
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016