Variant (rsID / SNP)

rs61749738

rs61749738 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.719C>G (p.Thr240Ser)
Allele change: Missense_T228S

Associated conditions / phenotypes

Severe neonatal-onset encephalopathy with microcephaly|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.