Variant (rsID / SNP)

rs41312157

rs41312157 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF81. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ZNF81Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: Xp11.23
HGVS: NM_007137.5(ZNF81):c.470A>G (p.Asn157Ser)
Allele change: Missense_N157S

Associated conditions / phenotypes

History of neurodevelopmental disorder

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.