Original source

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

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

Chromosome 8:132897729 (forward strand) | View in location tab

Co-located

with COSMIC COSM4162676 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2551 individual genotypes, is associated with 2 phenotypes and is mentioned in 3 citations.

Variation displays