Original source

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

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

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

Co-located

with HGMD-PUBLIC CM042760

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11227, 2009_August_001_212_PARK7_602533_0005

This variation has 18 HGVS names - click the plus to show

About this variant

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

Variation displays