Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.20 (T)
Location

Chromosome 3:58430808 (forward strand) | View in location tab

Co-located

with COSMIC COSM3760211 (C/T), COSM1047802 (C/A)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

This variant has 9 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 15 transcripts, has 2509 sample genotypes and is associated with 1 phenotype.

Variant displays