Variant (rsID / SNP)

rs63749027

rs63749027 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MECP2. The table records no clinical significance for this variant.

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Reference-table entries

MECP2Not classified

Variant type: Deletion
Cytoband: Xq28
HGVS: NM_001110792.2(MECP2):c.1268_1276del (p.Ser423_Cys425del)

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.