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rs121913267

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(ATCATGCATGAT;ATCATGCATGAT) 0 common in clinvar
Make rs121913267(-;-)
Make rs121913267(-;ATCATGCATGAT)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54285928
GenePDGFRA
is asnp
is mentioned by
dbSNPrs121913267
dbSNP (old)rs121913267
ClinGenrs121913267
ebirs121913267
HLIrs121913267
Exacrs121913267
Gnomadrs121913267
Varsomers121913267
Maprs121913267
PheGenIrs121913267
Biobankrs121913267
1000 genomesrs121913267
hgdprs121913267
ensemblrs121913267
gopubmedrs121913267
geneviewrs121913267
scholarrs121913267
googlers121913267
pharmgkbrs121913267
gwascentralrs121913267
openSNPrs121913267
23andMers121913267
23andMe allrs121913267
SNPshotrs121913267
SNPdbers121913267
MSV3drs121913267
GWAS Ctlgrs121913267
Max Magnitude0
ClinVar
Risk rs121913267(-;-)
Alt rs121913267(-;-)
Reference Rs121913267(ATCATGCATGAT;ATCATGCATGAT)
Significance Probable-Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene PDGFRA
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55152095_55152106delATCATGCATGAT
CLNSRC
CLNACC RCV000439347.1,