Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.33 (T)
Location

Chromosome 8:132971813 (forward strand) | View in location tab

Co-located

with COSMIC COSM3982409 (C/T) ; HGMD-PUBLIC CM035973

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 10 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 11 transcripts, has 2548 individual genotypes, is associated with 2 phenotypes and is mentioned in 4 citations.

Variation displays