Original source

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

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

Chromosome 16:23607914 (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 18 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 7 citations.

Variant displays