Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.27 (A)
Location

Chromosome 16:56993324 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs52828654, rs57153281

HGVS name

16:g.56993324C>A

This variation has assays on 10 chips - click the plus to show

Variation displays