RORB, RAR related orphan receptor B, 6096

N. diseases: 2; N. variants: 4
Source: CURATED ×
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: rs1327827
rs1327827 		9 74640194 non coding transcript exon variant T/C snv 0.86
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs35436838
rs35436838 		9 74658994 intron variant T/G snv 9.8E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs35436838
rs35436838 		9 74658994 intron variant T/G snv 9.8E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs55962158
rs55962158 		9 74627763 intron variant G/A;C;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs7042950
rs7042950 		1.000 9 74534921 intron variant A/G snv 0.27
CUI: C0034951
Disease: Refractive Errors
Refractive Errors 		Eye Diseases 0.700 1.000 1 2013 2013
dbSNP: rs7042950
rs7042950 		1.000 9 74534921 intron variant A/G snv 0.27
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction 		0.700 1.000 1 2013 2013