Variant (rsID / SNP)

rs17147624

rs17147624 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF41. Clinical significance in the table: Benign.

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Reference-table entries

ZNF41Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp11.3
HGVS: NM_001324144.2(ZNF41):c.374T>G (p.Ile125Arg)
Allele change: Missense_I159R

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.