Original source

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

Alleles
C/A/G | Ancestral: C | Ambiguity code: V
Location

Chromosome 5:151851420 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960777

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000171.3:c.882G>Y, 2268

This variation has 14 HGVS names - click the plus to show

Variation displays