Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S
Location

Chromosome 1:7965425 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM042760

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 11227, 2009_August_001_212_PARK7_602533_0005

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and is associated with 2 phenotypes.

Variant displays