Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.32 (T)
Location

Chromosome 8:132888007 (forward strand) | View in location tab

Co-located

with COSMIC COSM4162675 (T/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2515 individual genotypes, is associated with 2 phenotypes and is mentioned in 3 citations.

Variation displays