Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.33 (G)
Location

Chromosome 5:112840628 (forward strand)|View in location tab

Co-located variant

COSMIC COSM3760870

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 11 transcripts, has 3799 sample genotypes, is associated with 3 phenotypes and is mentioned in 10 citations.

Variant displays