Original source

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

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

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

Co-located

with HGMD-PUBLIC CM042452

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 15635, 2009_August_001_222_PINK1_608309_0005

This variant has 6 HGVS names - click the plus to show

About this variant

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

Variant displays