Variant (rsID / SNP)

rs132630304

rs132630304 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTM1. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MTM1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_000252.3(MTM1):c.205C>T (p.Arg69Cys)
Allele change: Missense_R69C

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.