Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variants
Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000007.12:g.2547482G>A

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and is mentioned in 1 citation.

Somatic mutation displays