Variant (rsID / SNP)

rs397516824

rs397516824 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAF1. Location: chromosome 3, position 12,660,155. Clinical significance in the table: Likely benign.

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Reference-table entries

RAF1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:12660155
Cytoband: 3p25.2
HGVS: NM_002880.4(RAF1):c.66T>G (p.Phe22Leu)
Allele change: Silent

Associated conditions / phenotypes

RASopathy

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.