Variant (rsID / SNP)

rs61753982

rs61753982 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MECP2. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MECP2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: Deletion
Cytoband: Xq28
HGVS: NM_001110792.2(MECP2):c.414-17del

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.