Variant (rsID / SNP)

rs61751452

rs61751452 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.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MECP2Not classified

Variant type: Deletion
Cytoband: Xq28
HGVS: NM_001110792.2(MECP2):c.1001_1006del (p.Pro334_Leu335del)

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.