Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.39 (T)
Location

Chromosome 16:3254573 (forward strand) | View in location tab

Co-located

with COSMIC COSM1128970 (G/T)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 17 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 15 transcripts, has 2557 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays