Variant (rsID / SNP)

rs182239885

rs182239885 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF81. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ZNF81Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Cytoband: Xp11.23
HGVS: NM_007137.5(ZNF81):c.1495A>G (p.Ile499Val)
Allele change: Missense_I499V

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.