SEMA4A, semaphorin 4A, 64218

N. diseases: 141; N. variants: 5
Disease: Autosomal dominant retinitis pigmentosa ×
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: rs41265017
rs41265017 		1.000 0.080 1 156176849 missense variant G/A snv 3.7E-02 3.2E-02
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.010 1.000 1 2018 2018