Variant (rsID / SNP)

rs187237351

rs187237351 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF674. Clinical significance in the table: Benign.

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Reference-table entries

ZNF674Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp11.3
HGVS: NM_001190417.2(ZNF674):c.884G>A (p.Arg295Gln)
Allele change: Missense_R294Q

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.