Have questions? Visit https://www.reddit.com/r/SNPedia

rs878854574

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854574(A;C)
Make rs878854574(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17033147
GeneSDHB
is asnp
is mentioned by
dbSNPrs878854574
ebirs878854574
HLIrs878854574
Exacrs878854574
Varsomers878854574
Maprs878854574
PheGenIrs878854574
hapmaprs878854574
1000 genomesrs878854574
hgdprs878854574
ensemblrs878854574
gopubmedrs878854574
geneviewrs878854574
scholarrs878854574
googlers878854574
pharmgkbrs878854574
gwascentralrs878854574
openSNPrs878854574
23andMers878854574
23andMe allrs878854574
SNP Nexus

SNPshotrs878854574
SNPdbers878854574
MSV3drs878854574
GWAS Ctlgrs878854574
Max Magnitude0
ClinVar
Risk rs878854574(C;C)
Alt rs878854574(C;C)
Reference rs878854574(A;A)
Significance Probable-Pathogenic
Disease Paraganglioma and gastric stromal sarcoma Paragangliomas 1 Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Paraganglioma and gastric stromal sarcoma Paragangliomas 1 Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17359642T>G
CLNSRC
CLNACC RCV000229229.1,