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Variant (rsID / SNP)

rs137960129

MFN2

rs137960129 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MFN2. Location: chromosome 1, position 12,059,092. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MFN2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:12059092
Cytoband
1p36.22
HGVS
NM_014874.4(MFN2):c.756C>T (p.Asn252=)
Allele change
Synonymous_N252N

Associated conditions / phenotypes

Hereditary motor and sensory neuropathy with optic atrophy|Charcot-Marie-Tooth disease type 2|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.