Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variant

HGMD-PUBLIC CM040493

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 4306, 2010_April_001_081_SNCA_163890_0004

HGVS names

This variant has 23 HGVS names - Show

About this variant

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

Variant displays