Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.18 (A)
Location

Chromosome 5:159387525 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs11135060, rs59372928

HGVS name

5:g.159387525A>C

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

Variation displays