Variant (rsID / SNP)

rs876658569

rs876658569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FH. Location: chromosome 1, position 241,676,965. Clinical significance in the table: Pathogenic.

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Reference-table entries

FHPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 1:241676965
Cytoband: 1q43
HGVS: NM_000143.4(FH):c.316del (p.Glu105_Val106insTer)

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Fumarase deficiency

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.