Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs52828654, rs57153281

HGVS name

16:g.56959412C>A

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

Variation displays