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rs878854590

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854590(-;-)
Make rs878854590(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position112088870
GeneSDHD
is asnp
is mentioned by
dbSNPrs878854590
ebirs878854590
HLIrs878854590
Exacrs878854590
Varsomers878854590
Maprs878854590
PheGenIrs878854590
hapmaprs878854590
1000 genomesrs878854590
hgdprs878854590
ensemblrs878854590
gopubmedrs878854590
geneviewrs878854590
scholarrs878854590
googlers878854590
pharmgkbrs878854590
gwascentralrs878854590
openSNPrs878854590
23andMers878854590
23andMe allrs878854590
SNP Nexus

SNPshotrs878854590
SNPdbers878854590
MSV3drs878854590
GWAS Ctlgrs878854590
Max Magnitude0
ClinVar
Risk rs878854590(;)
Alt rs878854590(;)
Reference rs878854590(G;G)
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.111959594delG
CLNSRC
CLNACC RCV000233424.1,