Original source

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

Alleles
A/C/T|Ancestral: A|Ambiguity code: H|MAF: 0.02 (C)
Location

Chromosome 16:23607914 (forward strand)|View in location tab

Co-located variant

COSMIC COSM5020553

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 20 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts, has 2505 sample genotypes, is associated with 3 phenotypes and is mentioned in 8 citations.

Variant displays