Variant (rsID / SNP)

rs3733540

rs3733540 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDGFRA. Location: chromosome 4, position 55,161,254. Clinical significance in the table: Benign.

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Reference-table entries

PDGFRABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:55161254
Cytoband: 4q12
HGVS: NM_006206.6(PDGFRA):c.3123-38C>T
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.