Original source

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

C/A | Ancestral: A | Ambiguity code: M | MAF: 0.26 (A)

Chromosome 16:28878165 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 17 transcripts, has 3691 sample genotypes, is associated with 2 phenotypes and is mentioned in 3 citations.

Variant displays