Original source

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

Alleles
C/A|Ancestral: A|Ambiguity code: M|MAF: 0.45 (C)
Location

Chromosome 16:56961324 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR000229

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

16:g.56961324C>A

Genotyping chips

This variant has assays on 15 chips - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 3964 sample genotypes, is associated with 8 phenotypes and is mentioned in 60 citations.

Variant displays