Original source

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

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

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

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

16:g.56959412C>A

This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 3691 sample genotypes, is associated with 26 phenotypes and is mentioned in 83 citations.

Variant displays