Disease: Hematocrit procedure ×
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: rs10224002
rs10224002 		0.925 0.080 7 151717955 intron variant A/G snv 0.31
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.800 1.000 1 2009 2009
dbSNP: rs10224210
rs10224210 		1.000 0.040 7 151716108 intron variant T/C snv 0.21
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 2 2016 2017