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rs190139590

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs190139590(A;T)
Make rs190139590(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position17028580
GeneSDHB
is asnp
is mentioned by
dbSNPrs190139590
ebirs190139590
HLIrs190139590
Exacrs190139590
Varsomers190139590
Maprs190139590
PheGenIrs190139590
hapmaprs190139590
1000 genomesrs190139590
hgdprs190139590
ensemblrs190139590
gopubmedrs190139590
geneviewrs190139590
scholarrs190139590
googlers190139590
pharmgkbrs190139590
gwascentralrs190139590
openSNPrs190139590
23andMers190139590
23andMe allrs190139590
SNP Nexus

SNPshotrs190139590
SNPdbers190139590
MSV3drs190139590
GWAS Ctlgrs190139590
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs190139590(T;T)
Alt rs190139590(T;T)
Reference rs190139590(A;A)
Significance Probable-Pathogenic
Disease Pheochromocytoma not specified Gastrointestinal stromal tumor Paragangliomas 4
Variation info
Gene SDHB
CLNDBN Pheochromocytoma not specified Gastrointestinal stromal tumor Paragangliomas 4
Reversed 0
HGVS NC_000001.10:g.17355075A>T
CLNSRC ClinVar
CLNACC RCV000030448.1, RCV000183209.2, RCV000204733.2,


[PMID 18419787] Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B (SDH-B) gene mutation carriers.