Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.20 (A)
Location

Chromosome 16:58634662 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58902631, rs183758

HGVS name

16:g.58634662G>A

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

Variation displays