Original source

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

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS name

16:g.56959412C>A

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