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rs878854589

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878854589(-;-)
Make rs878854589(-;C)
Make rs878854589(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position112086917
GeneSDHD, TIMM8B
is asnp
is mentioned by
dbSNPrs878854589
ebirs878854589
HLIrs878854589
Exacrs878854589
Varsomers878854589
Maprs878854589
PheGenIrs878854589
hapmaprs878854589
1000 genomesrs878854589
hgdprs878854589
ensemblrs878854589
gopubmedrs878854589
geneviewrs878854589
scholarrs878854589
googlers878854589
pharmgkbrs878854589
gwascentralrs878854589
openSNPrs878854589
23andMers878854589
23andMe allrs878854589
SNP Nexus

SNPshotrs878854589
SNPdbers878854589
MSV3drs878854589
GWAS Ctlgrs878854589
Max Magnitude0
ClinVar
Risk rs878854589(C;C)
Alt rs878854589(C;C)
Reference rs878854589(;)
Significance Pathogenic
Disease Paraganglioma and gastric stromal sarcoma Paragangliomas 1 Pheochromocytoma
Variation info
Gene TIMM8B SDHD
CLNDBN Paraganglioma and gastric stromal sarcoma Paragangliomas 1 Pheochromocytoma
Reversed 0
HGVS NC_000011.9:g.111957641dupC
CLNSRC
CLNACC RCV000232971.1,