Original source

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

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

Chromosome 16:88504451 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

LSDB ZNF469_c.10489G>A

This variation has 5 HGVS names - click the plus to show

Variation displays