Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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

Variation displays