Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.46 (G)
Location

Chromosome 16:28483029 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 33 HGVS names - click the plus to show

Variation displays