Variant (rsID / SNP)

rs12069578

rs12069578 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MFN2. Location: chromosome 1, position 12,064,067. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MFN2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:12064067
Cytoband: 1p36.22
HGVS: NM_014874.4(MFN2):c.1179G>A (p.Met393Ile)
Allele change: Missense_M393I

Associated conditions / phenotypes

Charcot-Marie-Tooth disease type 2|Charcot-Marie-Tooth disease

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.