Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 4:89828149 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971400

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4303, 2010_April_001_079_SNCA_163890_0001

This variation has 23 HGVS names - click the plus to show

Variation displays