Original source

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

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

Chromosome 1:20645640 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM042452

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 15635, 2009_August_001_222_PINK1_608309_0005

HGVS names

This variant has 6 HGVS names - Show

About this variant

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

Variant displays