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rs878854591

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854591(-;-)
Make rs878854591(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position112088939
GeneSDHD
is asnp
is mentioned by
dbSNPrs878854591
ebirs878854591
HLIrs878854591
Exacrs878854591
Varsomers878854591
Maprs878854591
PheGenIrs878854591
hapmaprs878854591
1000 genomesrs878854591
hgdprs878854591
ensemblrs878854591
gopubmedrs878854591
geneviewrs878854591
scholarrs878854591
googlers878854591
pharmgkbrs878854591
gwascentralrs878854591
openSNPrs878854591
23andMers878854591
23andMe allrs878854591
SNP Nexus

SNPshotrs878854591
SNPdbers878854591
MSV3drs878854591
GWAS Ctlgrs878854591
Max Magnitude0
ClinVar
Risk rs878854591(;)
Alt rs878854591(;)
Reference rs878854591(C;C)
Significance 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.111959663delC
CLNSRC
CLNACC RCV000228216.1,