Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.36 (C)

Chromosome 16:3247181 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 27 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 16 transcripts, has 2589 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variant displays