This variation has been flagged

Flagged as suspect by dbSNP

Original source

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

A/G | Ancestral: A | Ambiguity code: R

Chromosome 16:50786182 (forward strand) | View in location tab

Most severe consequence

This variation has 14 HGVS names - click the plus to show

Variation displays