Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 1:20649054 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041052

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_219_PINK1_608309_0002, 15632

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

About this variant

This variant overlaps 8 transcripts and is associated with 2 phenotypes.

Variant displays