Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 1:20644526 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM042450

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_221_PINK1_608309_0004, 15634

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays