Variant (rsID / SNP)

rs104894955

rs104894955 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF41. Clinical significance in the table: Likely benign.

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Reference-table entries

ZNF41Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Cytoband: Xp11.3
HGVS: NM_001324144.2(ZNF41):c.332C>T (p.Pro111Leu)
Allele change: Missense_P145L

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.