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Variant (rsID / SNP)

rs200542051

FH

rs200542051 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FH. Location: chromosome 1, position 241,682,990. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FHConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:241682990
Cytoband
1q43
HGVS
NM_000143.4(FH):c.33G>C (p.Ser11=)
Allele change
Synonymous_S11S

Associated conditions / phenotypes

Fumarase deficiency|Hereditary leiomyomatosis and renal cell cancer|Hereditary cancer-predisposing syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.