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rs35597368

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs35597368(C;C)
Make rs35597368(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position54273604
GenePDGFRA
is asnp
is mentioned by
dbSNPrs35597368
ebirs35597368
HLIrs35597368
Exacrs35597368
Varsomers35597368
Maprs35597368
PheGenIrs35597368
hapmaprs35597368
1000 genomesrs35597368
hgdprs35597368
ensemblrs35597368
gopubmedrs35597368
geneviewrs35597368
scholarrs35597368
googlers35597368
pharmgkbrs35597368
gwascentralrs35597368
openSNPrs35597368
23andMers35597368
23andMe allrs35597368
SNP Nexus

SNPshotrs35597368
SNPdbers35597368
MSV3drs35597368
GWAS Ctlgrs35597368
GMAF0.1653
Max Magnitude0

[PMID 22015057] Single nucleotide polymorphism associations with response and toxic effects in patients with advanced renal-cell carcinoma treated with first-line sunitinib: a multicentre, observational, prospective study


GET Evidence
PDGFRA-S478P
aa_change Ser478Pro
aa_change_short S478P
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.14473
summary



ClinVar
Risk rs35597368(C;C)
Alt rs35597368(C;C)
Reference rs35597368(T;T)
Significance Non-pathogenic
Disease not provided not specified
Variation info
Gene PDGFRA
CLNDBN not provided not specified
Reversed 0
HGVS NC_000004.11:g.55139771T>C
CLNSRC ClinVar
CLNACC RCV000034716.1, RCV000121780.1,



[PMID 26254278OA-icon.png] Impact of VEGF, VEGFR, PDGFR, HIF and ERCC1 gene polymorphisms on thymic malignancies outcome after thymectomy