Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.47 (C)
Location

Chromosome 13:51949672 (forward strand) | View in location tab

Co-located

with COSMIC COSM147691 (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 8 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 4271 individual genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variation displays