HOXC12, homeobox C12, 3228

N. diseases: 5; N. variants: 3
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: rs10783615
rs10783615 		12 53955989 intron variant G/A snv 0.71
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs10783615
rs10783615 		12 53955989 intron variant G/A snv 0.71
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs894739
rs894739 		12 53953085 upstream gene variant T/C snv 0.65
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs189468720
rs189468720 		0.925 0.080 12 53955457 missense variant C/G snv 3.6E-03 3.6E-03
CUI: C0240912
Disease: Vertical Talus
Vertical Talus 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2016 2016
dbSNP: rs189468720
rs189468720 		0.925 0.080 12 53955457 missense variant C/G snv 3.6E-03 3.6E-03
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2016 2016