Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

with COSMIC COSM3760870 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 2625 individual genotypes, is associated with 1 phenotype and is mentioned in 10 citations.

Variation displays