PHC2, polyhomeotic homolog 2, 1912

N. diseases: 9; N. variants: 5
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: rs10914684
rs10914684 		1 33329971 intron variant G/A snv 0.25
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4653102
rs4653102 		1 33364812 intron variant T/C snv 0.62
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs55745410
rs55745410 		1 33337216 intron variant A/G snv 0.28
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs55745410
rs55745410 		1 33337216 intron variant A/G snv 0.28
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs72658302
rs72658302 		1 33418145 intron variant T/C snv 9.8E-02
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs72660103
rs72660103 		1 33420920 intron variant C/T snv 9.5E-02
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2018 2018