Original source

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

C/A|Ancestral: C|Ambiguity code: M|MAF: 0.29 (A)

Chromosome 16:56959412 (forward strand)|View in location tab

Most severe consequence
Upstream gene variant
Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS name


Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 5 transcripts, has 3691 sample genotypes, is associated with 28 phenotypes and is mentioned in 90 citations.

Variant displays