PHC3, polyhomeotic homolog 3, 80012

N. diseases: 10; N. variants: 2
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: rs6808506
rs6808506 		3 170121451 intron variant G/C snv 0.11
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs73181210
rs73181210 		3 170113480 missense variant T/C snv 6.0E-03 5.2E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs73181210
rs73181210 		3 170113480 missense variant T/C snv 6.0E-03 5.2E-03
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019