Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 variant

COSMIC COSM3763989

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

This variant has 5 synonyms - Show

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - 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