Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 16:88430169 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB ZNF469_c.2699C>T

This variation has 10 HGVS names - click the plus to show

Variation displays