Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G/T | Ancestral: C | Ambiguity code: B | MAF: < 0.01 (T)
Location

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB ZNF469_c.2699C>T, ZNF469_c.2699C>G

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

About this variant

This variant overlaps 5 transcripts, has 2504 individual genotypes and is associated with 2 phenotypes.

Variation displays