Variant (rsID / SNP)

rs369635503

rs369635503 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRAF. Location: chromosome 7, position 140,477,894. Clinical significance in the table: Benign.

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Reference-table entries

BRAFBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:140477894
Cytoband: 7q34
HGVS: NM_004333.6(BRAF):c.1433-19A>G
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.