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rs878854575

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854575(A;T)
Make rs878854575(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17033075
GeneSDHB
is asnp
is mentioned by
dbSNPrs878854575
ebirs878854575
HLIrs878854575
Exacrs878854575
Varsomers878854575
Maprs878854575
PheGenIrs878854575
hapmaprs878854575
1000 genomesrs878854575
hgdprs878854575
ensemblrs878854575
gopubmedrs878854575
geneviewrs878854575
scholarrs878854575
googlers878854575
pharmgkbrs878854575
gwascentralrs878854575
openSNPrs878854575
23andMers878854575
23andMe allrs878854575
SNP Nexus

SNPshotrs878854575
SNPdbers878854575
MSV3drs878854575
GWAS Ctlgrs878854575
Max Magnitude0
ClinVar
Risk rs878854575(T;T)
Alt rs878854575(T;T)
Reference rs878854575(A;A)
Significance Pathogenic
Disease Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17359570T>A
CLNSRC
CLNACC RCV000230068.1,