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: 0.25 (A)
Location

Chromosome 19:48393986 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57555058, rs1799276

HGVS name

19:g.48393986C>A

This variation has assays on 5 chips - click the plus to show

Variation displays