Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 4:89828170 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM040493

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 4306, 2010_April_001_081_SNCA_163890_0004

This variant has 23 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and is associated with 2 phenotypes.

Variant displays