rs35597368

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs35597368(C;C)

Make rs35597368(C;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

54273604

Gene

PDGFRA

is a	snp
is	mentioned by
dbSNP	rs35597368
dbSNP (classic)	rs35597368
ClinGen	rs35597368
ebi	rs35597368
HLI	rs35597368
Exac	rs35597368
Gnomad	rs35597368
Varsome	rs35597368
LitVar	rs35597368
Map	rs35597368
PheGenI	rs35597368
Biobank	rs35597368
1000 genomes	rs35597368
hgdp	rs35597368
ensembl	rs35597368
geneview	rs35597368
scholar	rs35597368
google	rs35597368
pharmgkb	rs35597368
gwascentral	rs35597368
openSNP	rs35597368
23andMe	rs35597368
SNPshot	rs35597368
SNPdbe	rs35597368
MSV3d	rs35597368
GWAS Ctlg	rs35597368

GMAF

0.1653

Max Magnitude

0

[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

ClinVar
Risk	rs35597368(C;C)
Alt	rs35597368(C;C)
Reference	Rs35597368(T;T)
Significance	Non-pathogenic
Disease	not provided not specified Gastrointestinal stromal tumor Idiopathic hypereosinophilic syndrome
Variation	info
Gene	PDGFRA
CLNDBN	not provided not specified Gastrointestinal stromal tumor Idiopathic hypereosinophilic syndrome
Reversed	0
HGVS	NC_000004.11:g.55139771T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000034716.1, RCV000121780.2, RCV000326887.1, RCV000381487.1,

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