Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 6 chips - click the plus to 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