Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

Chromosome 16:88438043 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB ZNF469_c.10489G>A

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and is associated with 1 phenotype.

Variant displays