Variant (rsID / SNP)

rs119103265

rs119103265 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MFN2. Location: chromosome 1, position 12,062,090. Clinical significance in the table: Pathogenic.

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Reference-table entries

MFN2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:12062090
Cytoband: 1p36.22
HGVS: NM_014874.4(MFN2):c.1090C>T (p.Arg364Trp)
Allele change: Missense_R364W

Associated conditions / phenotypes

Hereditary motor and sensory neuropathy with optic atrophy|Charcot-Marie-Tooth disease type 2A2|Charcot-Marie-Tooth disease type 2|Charcot-Marie-Tooth disease|Charcot-Marie-Tooth disease type 4

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.