Original source

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

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

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

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

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