Variant (rsID / SNP)

rs77524207

rs77524207 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDGFRA. Location: chromosome 4, position 55,133,806. 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: 4:55133806
Cytoband: 4q12
HGVS: NM_006206.6(PDGFRA):c.1019G>A (p.Arg340Gln)
Allele change: Missense_R340Q

Associated conditions / phenotypes

Gastrointestinal stromal tumor|Idiopathic hypereosinophilic syndrome|Hereditary cancer-predisposing syndrome

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.