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rs397516833

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516833(C;C)
Make rs397516833(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position17028737
GeneSDHB
is asnp
is mentioned by
dbSNPrs397516833
ebirs397516833
HLIrs397516833
Exacrs397516833
Varsomers397516833
Maprs397516833
PheGenIrs397516833
hapmaprs397516833
1000 genomesrs397516833
hgdprs397516833
ensemblrs397516833
gopubmedrs397516833
geneviewrs397516833
scholarrs397516833
googlers397516833
pharmgkbrs397516833
gwascentralrs397516833
openSNPrs397516833
23andMers397516833
23andMe allrs397516833
SNP Nexus

SNPshotrs397516833
SNPdbers397516833
MSV3drs397516833
GWAS Ctlgrs397516833
Max Magnitude0
ClinVar
Risk rs397516833(C;C)
Alt rs397516833(C;C)
Reference rs397516833(G;G)
Significance Pathogenic
Disease Hereditary Paraganglioma-Pheochromocytoma Syndromes Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary Paraganglioma-Pheochromocytoma Syndromes Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17355232C>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000037719.2, RCV000128907.2,