Original source

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

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

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

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


Archive dbSNP rs57201603, rs2228992

HGVS names

This variant has 3 HGVS names - 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