Original source

Variants (including SNPs and indels) imported from dbSNP (release 139) | [View in dbSNP]

Alleles
G/A | Ambiguity code: R
Location

Chromosome 16:8789496 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

Variation displays