Variant (rsID / SNP)

rs11923054

rs11923054 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZBBX. Location: chromosome 3, position 167,051,769. The table records no clinical significance for this variant.

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Reference-table entries

ZBBXNot classified

Variant type: missense_variant
Chromosome / position: 3:167051769
HGVS: NM_001199201.2,c.533A>G,p.Lys178Arg
Allele change: Missense_K178R

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.