Variant (rsID / SNP)

rs62636526

rs62636526 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLT3. Location: chromosome 13, position 28,644,747. Clinical significance in the table: Likely benign.

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Reference-table entries

FLT3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 13:28644747
Cytoband: 13q12.2
HGVS: NM_004119.3(FLT3):c.46G>C (p.Val16Leu)
Allele change: Silent

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.