Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.33 (G)
Location

Chromosome 19:10289628 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs827787, rs61116170, rs3760652

HGVS name

19:g.10289628G>A

This variation has assays on 11 chips - click the plus to show

Variation displays