Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.45 (A)
Location

Chromosome 1:16992516 (forward strand) | View in location tab

Co-located

with COSMIC COSM3997075 (G/A), COSM3997076 (G/A)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs117976713

This variant has 6 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 12 transcripts, has 2549 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays