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rs121908589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908589(A;G)
Make rs121908589(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position54274851
GenePDGFRA
is asnp
is mentioned by
dbSNPrs121908589
ebirs121908589
HLIrs121908589
Exacrs121908589
Varsomers121908589
Maprs121908589
PheGenIrs121908589
hapmaprs121908589
1000 genomesrs121908589
hgdprs121908589
ensemblrs121908589
gopubmedrs121908589
geneviewrs121908589
scholarrs121908589
googlers121908589
pharmgkbrs121908589
gwascentralrs121908589
openSNPrs121908589
23andMers121908589
23andMe allrs121908589
SNP Nexus

SNPshotrs121908589
SNPdbers121908589
MSV3drs121908589
GWAS Ctlgrs121908589
Max Magnitude0
OMIM173490
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121908589(G;G)
Alt rs121908589(G;G)
Reference rs121908589(A;A)
Significance Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene PDGFRA
CLNDBN Gastrointestinal stromal tumor, familial
Reversed 0
HGVS NC_000004.11:g.55141018A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014511.24,