Source: GWASDB

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: rs445
rs445
7 92779056 intron variant C/T snv 0.14
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.800 1.000 1 2011 2019
dbSNP: rs445
rs445
7 92779056 intron variant C/T snv 0.14
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.800 1.000 1 2010 2019