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: 0.38 (G)
Location

Chromosome 10:23191389 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58290468

HGVS name

10:g.23191389G>A

This variation has assays on 4 chips - click the plus to show

Variation displays