Variant (rsID / SNP)

rs187912365

rs187912365 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RB1. Location: chromosome 13, position 49,039,407. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RB1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 13:49039407
Cytoband: 13q14.2
HGVS: NM_000321.3(RB1):c.2392C>T (p.Arg798Trp)
Allele change: Missense_R798W

Associated conditions / phenotypes

Retinoblastoma|Hereditary cancer-predisposing syndrome

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.