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rs121913262

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GACATCATG;GACATCATG) 0 common in clinvar
Make rs121913262(-;-)
Make rs121913262(-;GACATCATG)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54285925
GenePDGFRA
is asnp
is mentioned by
dbSNPrs121913262
dbSNP (old)rs121913262
ClinGenrs121913262
ebirs121913262
HLIrs121913262
Exacrs121913262
Gnomadrs121913262
Varsomers121913262
Maprs121913262
PheGenIrs121913262
Biobankrs121913262
1000 genomesrs121913262
hgdprs121913262
ensemblrs121913262
gopubmedrs121913262
geneviewrs121913262
scholarrs121913262
googlers121913262
pharmgkbrs121913262
gwascentralrs121913262
openSNPrs121913262
23andMers121913262
23andMe allrs121913262
SNPshotrs121913262
SNPdbers121913262
MSV3drs121913262
GWAS Ctlgrs121913262
Max Magnitude0
ClinVar
Risk rs121913262(-;-)
Alt rs121913262(-;-)
Reference Rs121913262(GACATCATG;GACATCATG)
Significance Probable-Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene PDGFRA
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55152092_55152100delGACATCATG
CLNSRC
CLNACC RCV000421502.1,