Variant (rsID / SNP)

rs587783752

rs587783752 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTM1. Clinical significance in the table: Pathogenic.

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Reference-table entries

MTM1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Cytoband: Xq28
HGVS: NM_000252.3(MTM1):c.1088_1089del (p.Lys363fs)

Associated conditions / phenotypes

Severe X-linked myotubular myopathy

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.