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rs121913271

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGCCCAGATGGACATGAA;AGCCCAGATGGACATGAA) 0 common in clinvar
Make rs121913271(AGCCCAGATGGACATGAA;CGC)
Make rs121913271(CGC;CGC)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position54274883
GenePDGFRA
is asnp
is mentioned by
dbSNPrs121913271
dbSNP (old)rs121913271
ClinGenrs121913271
ebirs121913271
HLIrs121913271
Exacrs121913271
Varsomers121913271
Maprs121913271
PheGenIrs121913271
Biobankrs121913271
1000 genomesrs121913271
hgdprs121913271
ensemblrs121913271
gopubmedrs121913271
geneviewrs121913271
scholarrs121913271
googlers121913271
pharmgkbrs121913271
gwascentralrs121913271
openSNPrs121913271
23andMers121913271
23andMe allrs121913271
SNP Nexus

SNPshotrs121913271
SNPdbers121913271
MSV3drs121913271
GWAS Ctlgrs121913271
Max Magnitude0
ClinVar
Risk rs121913271(CGC;CGC)
Alt rs121913271(CGC;CGC)
Reference Rs121913271(AGCCCAGATGGACATGAA;AGCCCAGATGGACATGAA)
Significance Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene PDGFRA
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55141050_55141067del18
CLNSRC OMIM Allelic Variant
CLNACC RCV000014508.4,