Original source

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

T/A/C|Ancestral: C|Ambiguity code: H|MAF: 0.39 (C)

Chromosome 16:3254654 (forward strand)|View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 46 HGVS names - Show

About this variant

This variant overlaps 30 transcripts, has 2567 sample genotypes, is associated with 2 phenotypes and is mentioned in 4 citations.

Variant displays