Variant (rsID / SNP)

rs371846795

rs371846795 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAF1. Location: chromosome 3, position 12,647,694. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

RAF1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:12647694
Cytoband: 3p25.2
HGVS: NM_002880.4(RAF1):c.680+6T>C
Allele change: Silent

Associated conditions / phenotypes

LEOPARD syndrome 2|Noonan syndrome 5|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.