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: 0.21 (A)
Location

Chromosome 4:56393299 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3172571, rs58158009

HGVS name

4:g.56393299C>A

This variation has assays on 7 chips - click the plus to show

Variation displays