Original source

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

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

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

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

16:g.28878165C>A

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