Original source

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

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

Chromosome 5:35871088 (forward strand)|View in location tab

Co-located variant

COSMIC COSM149814

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 10 synonyms - Show

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 9 transcripts, has 4492 sample genotypes, is associated with 3 phenotypes and is mentioned in 22 citations.

Variant displays