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rs606231209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGCCCAGATGGACATGAA;AGCCCAGATGGACATGAA) 0 common in clinvar
Make rs606231209(-;-)
Make rs606231209(-;AGCCCAGATGGACATGAA)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position54274883
GenePDGFRA
is asnp
is mentioned by
dbSNPrs606231209
ClinGenrs606231209
ebirs606231209
HLIrs606231209
Exacrs606231209
Varsomers606231209
Maprs606231209
PheGenIrs606231209
Biobankrs606231209
1000 genomesrs606231209
hgdprs606231209
ensemblrs606231209
gopubmedrs606231209
geneviewrs606231209
scholarrs606231209
googlers606231209
pharmgkbrs606231209
gwascentralrs606231209
openSNPrs606231209
23andMers606231209
23andMe allrs606231209
SNP Nexus

SNPshotrs606231209
SNPdbers606231209
MSV3drs606231209
GWAS Ctlgrs606231209
Max Magnitude0
ClinVar
Risk rs606231209(-;-)
Alt rs606231209(-;-)
Reference Rs606231209(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,