Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.15 (G)
Location

Chromosome 16:23215466 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs57201603, rs2228992

This variant has 2 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 2909 sample genotypes, is associated with 1 phenotype and is mentioned in 6 citations.

Variant displays