Original source

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

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

Chromosome 4:89835580 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981851

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4304, 2010_April_001_080_SNCA_163890_0002

This variation has 27 HGVS names - click the plus to show

Variation displays