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: rs184088518
rs184088518
EGLN2 ; RAB4B-EGLN2
19 40799233 5 prime UTR variant G/T snv 1.8E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs61750953
rs61750953
EGLN2 ; RAB4B-EGLN2
19 40800745 missense variant C/T snv 1.6E-02 1.4E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016