Variant (rsID / SNP)

rs61752361

rs61752361 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MECP2. Clinical significance in the table: Benign.

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Reference-table entries

MECP2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_001110792.2(MECP2):c.1066C>T (p.Arg356Trp)
Allele change: Missense_R344W

Associated conditions / phenotypes

Rett syndrome|Severe neonatal-onset encephalopathy with microcephaly

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.