Original source

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

G/A | Ambiguity code: R

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

Most severe consequence
Missense variant
Evidence status

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

About this variant

This variant overlaps 1 transcript.

Variant displays