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rs878854594

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854594(C;T)
Make rs878854594(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position112094851
GeneSDHD
is asnp
is mentioned by
dbSNPrs878854594
ebirs878854594
HLIrs878854594
Exacrs878854594
Varsomers878854594
Maprs878854594
PheGenIrs878854594
hapmaprs878854594
1000 genomesrs878854594
hgdprs878854594
ensemblrs878854594
gopubmedrs878854594
geneviewrs878854594
scholarrs878854594
googlers878854594
pharmgkbrs878854594
gwascentralrs878854594
openSNPrs878854594
23andMers878854594
23andMe allrs878854594
SNP Nexus

SNPshotrs878854594
SNPdbers878854594
MSV3drs878854594
GWAS Ctlgrs878854594
Max Magnitude0
ClinVar
Risk rs878854594(T;T)
Alt rs878854594(T;T)
Reference rs878854594(C;C)
Significance Probable-Pathogenic
Disease Paraganglioma and gastric stromal sarcoma Paragangliomas 1 Pheochromocytoma
Variation info
Gene SDHD
CLNDBN Paraganglioma and gastric stromal sarcoma Paragangliomas 1 Pheochromocytoma
Reversed 0
HGVS NC_000011.9:g.111965575C>T
CLNSRC
CLNACC RCV000226232.1,