SLC35A2, solute carrier family 35 member A2, 7355

N. diseases: 197; N. variants: 18
Disease: Cerebral white matter atrophy ×
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: rs1557043622
rs1557043622 		0.695 0.400 X 48909843 missense variant C/A snv
CUI: C4022735
Disease: Cerebral white matter atrophy
Cerebral white matter atrophy 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019