RXRA, retinoid X receptor alpha, 6256

N. diseases: 132; N. variants: 23
Disease: Huntington Disease ×
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: rs10881578
rs10881578 		0.925 0.240 9 134340689 intron variant A/G snv 0.32
CUI: C0020179
Disease: Huntington Disease
Huntington Disease 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders 0.010 1.000 1 2018 2018