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rs587782604

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782604(A;A)
Make rs587782604(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position17022684
GeneSDHB
is asnp
is mentioned by
dbSNPrs587782604
ClinGenrs587782604
ebirs587782604
HLIrs587782604
Exacrs587782604
Varsomers587782604
Maprs587782604
PheGenIrs587782604
hapmaprs587782604
1000 genomesrs587782604
hgdprs587782604
ensemblrs587782604
gopubmedrs587782604
geneviewrs587782604
scholarrs587782604
googlers587782604
pharmgkbrs587782604
gwascentralrs587782604
openSNPrs587782604
23andMers587782604
23andMe allrs587782604
SNP Nexus

SNPshotrs587782604
SNPdbers587782604
MSV3drs587782604
GWAS Ctlgrs587782604
Max Magnitude0
ClinVar
Risk rs587782604(A;A) rs587782604(T;T)
Alt rs587782604(A;A) rs587782604(T;T)
Reference Rs587782604(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma not provided
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma not provided
Reversed 1
HGVS NC_000001.10:g.17349179C>A; NC_000001.10:g.17349179C>T
CLNSRC
CLNACC RCV000164275.2, RCV000473831.1, RCV000131970.4, RCV000183215.3, RCV000456660.1,