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rs121908585

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121908585(A;T)
Make rs121908585(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position54285926
GenePDGFRA
is asnp
is mentioned by
dbSNPrs121908585
ebirs121908585
HLIrs121908585
Exacrs121908585
Varsomers121908585
Maprs121908585
PheGenIrs121908585
hapmaprs121908585
1000 genomesrs121908585
hgdprs121908585
ensemblrs121908585
gopubmedrs121908585
geneviewrs121908585
scholarrs121908585
googlers121908585
pharmgkbrs121908585
gwascentralrs121908585
openSNPrs121908585
23andMers121908585
23andMe allrs121908585
SNP Nexus

SNPshotrs121908585
SNPdbers121908585
MSV3drs121908585
GWAS Ctlgrs121908585
Max Magnitude0
OMIM173490
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908585(T;T)
Alt rs121908585(T;T)
Reference rs121908585(A;A)
Significance Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene PDGFRA
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55152093A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014501.5,