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rs121913265

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913265(G;T)
Make rs121913265(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54285925
GenePDGFRA
is asnp
is mentioned by
dbSNPrs121913265
dbSNP (old)rs121913265
ClinGenrs121913265
ebirs121913265
HLIrs121913265
Exacrs121913265
Gnomadrs121913265
Varsomers121913265
Maprs121913265
PheGenIrs121913265
Biobankrs121913265
1000 genomesrs121913265
hgdprs121913265
ensemblrs121913265
gopubmedrs121913265
geneviewrs121913265
scholarrs121913265
googlers121913265
pharmgkbrs121913265
gwascentralrs121913265
openSNPrs121913265
23andMers121913265
23andMe allrs121913265
SNPshotrs121913265
SNPdbers121913265
MSV3drs121913265
GWAS Ctlgrs121913265
Max Magnitude0
ClinVar
Risk rs121913265(T;T)
Alt rs121913265(T;T)
Reference Rs121913265(G;G)
Significance Probable-Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene PDGFRA
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55152092G>T
CLNSRC
CLNACC RCV000439137.1,