Original source

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

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

Chromosome 7:2541322 (forward strand) | View in location tab

Co-located

with COSMIC COSM106599 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000007.12:g.2547482G>A

This variation has 11 HGVS names - click the plus to show

Variation displays