Variant (rsID / SNP)

rs267607246

rs267607246 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MPZ. Location: chromosome 1, position 161,276,217. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MPZUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:161276217
Cytoband: 1q23.3
HGVS: NM_000530.8(MPZ):c.486C>G (p.Ile162Met)
Allele change: Missense_I162M

Associated conditions / phenotypes

Charcot-Marie-Tooth disease, type I

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.