Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.49 (C)
Location

Chromosome 9:72688737 (forward strand) | View in location tab

Co-located

with COSMIC COSM3763989 (C/T)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

This variant has 5 synonyms - click the plus to show

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

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 4034 sample genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variant displays