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rs587776794

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776794(-;-)
Make rs587776794(-;AGAGGG)
Make rs587776794(AGAGGG;AGAGGG)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position54274868
GenePDGFRA
is asnp
is mentioned by
dbSNPrs587776794
ebirs587776794
HLIrs587776794
Exacrs587776794
Varsomers587776794
Maprs587776794
PheGenIrs587776794
hapmaprs587776794
1000 genomesrs587776794
hgdprs587776794
ensemblrs587776794
gopubmedrs587776794
geneviewrs587776794
scholarrs587776794
googlers587776794
pharmgkbrs587776794
gwascentralrs587776794
openSNPrs587776794
23andMers587776794
23andMe allrs587776794
SNP Nexus

SNPshotrs587776794
SNPdbers587776794
MSV3drs587776794
GWAS Ctlgrs587776794
Max Magnitude0
ClinVar
Risk rs587776794(GAGGGA;GAGGGA)
Alt rs587776794(GAGGGA;GAGGGA)
Reference rs587776794(;)
Significance Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene PDGFRA
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55141035_55141036insAGAGGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000014506.4,