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Variant (rsID / SNP)

rs267607241

MPZ

rs267607241 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MPZ. Location: chromosome 1, position 161,276,605. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MPZConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:161276605
Cytoband
1q23.3
HGVS
NM_000530.8(MPZ):c.341T>C (p.Ile114Thr)
Allele change
Missense_I114T

Associated conditions / phenotypes

Charcot-Marie-Tooth disease, type I|Charcot-Marie-Tooth disease

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.