Variant (rsID / SNP)

rs1933437

rs1933437 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLT3. Location: chromosome 13, position 28,624,294. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FLT3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:28624294
Cytoband: 13q12.2
HGVS: NM_004119.3(FLT3):c.680C>T (p.Thr227Met)
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.