Variant (rsID / SNP)

rs201874958

rs201874958 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDGFRA. Location: chromosome 4, position 55,156,697. Clinical significance in the table: Likely benign.

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Reference-table entries

PDGFRALikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:55156697
Cytoband: 4q12
HGVS: NM_006206.6(PDGFRA):c.3098A>T (p.Asp1033Val)
Allele change: Missense_D1058V

Associated conditions / phenotypes

Gastrointestinal stromal tumor

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.