FOLR3, folate receptor gamma, 2352

N. diseases: 8; N. variants: 5
Disease: Meningomyelocele ×
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: rs7926875
rs7926875 		1.000 0.080 11 72138396 intron variant C/A snv 6.9E-02
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.010 1.000 1 2010 2010