Variant (rsID / SNP)

rs117196884

rs117196884 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SUFU. Location: chromosome 10, position 104,391,584. Clinical significance in the table: Likely benign.

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Reference-table entries

SUFULikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:104391584
Cytoband: 10q24.32
HGVS: NM_016169.4(SUFU):c.*1672A>G
Allele change: Silent

Associated conditions / phenotypes

Medulloblastoma

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.