Variant (rsID / SNP)

rs62640397

rs62640397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FDX2. Location: chromosome 19, position 10,426,597. Clinical significance in the table: Benign.

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Reference-table entries

FDX2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:10426597
Cytoband: 19p13.2
HGVS: NM_001397406.1(FDX2):c.76A>G (p.Arg26Gly)
Allele change: Missense_R29G

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.