Original source

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

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

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

Co-located variant

COSMIC COSM1047802

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 13 HGVS names - 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