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rs121913264

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs121913264(AT;AT)
Make rs121913264(AT;GA)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54285925
GenePDGFRA
is asnp
is mentioned by
dbSNPrs121913264
dbSNP (old)rs121913264
ClinGenrs121913264
ebirs121913264
HLIrs121913264
Exacrs121913264
Gnomadrs121913264
Varsomers121913264
Maprs121913264
PheGenIrs121913264
Biobankrs121913264
1000 genomesrs121913264
hgdprs121913264
ensemblrs121913264
gopubmedrs121913264
geneviewrs121913264
scholarrs121913264
googlers121913264
pharmgkbrs121913264
gwascentralrs121913264
openSNPrs121913264
23andMers121913264
23andMe allrs121913264
SNPshotrs121913264
SNPdbers121913264
MSV3drs121913264
GWAS Ctlgrs121913264
Max Magnitude0
ClinVar
Risk rs121913264(AT;AT)
Alt rs121913264(AT;AT)
Reference Rs121913264(GA;GA)
Significance Probable-Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene PDGFRA
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55152092_55152093delGAinsAT
CLNSRC
CLNACC RCV000437652.1,