Variant (rsID / SNP)

rs886039368

rs886039368 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FH. Location: chromosome 1, position 241,661,161. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

FHPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:241661161
Cytoband: 1q43
HGVS: NM_000143.4(FH):c.1500G>A (p.Trp500Ter)
Allele change: Nonsense_W500X

Associated conditions / phenotypes

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

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.