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rs267607032

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607032(G;T)
Make rs267607032(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position17028605
GeneSDHB
is asnp
is mentioned by
dbSNPrs267607032
ebirs267607032
HLIrs267607032
Exacrs267607032
Varsomers267607032
Maprs267607032
PheGenIrs267607032
hapmaprs267607032
1000 genomesrs267607032
hgdprs267607032
ensemblrs267607032
gopubmedrs267607032
geneviewrs267607032
scholarrs267607032
googlers267607032
pharmgkbrs267607032
gwascentralrs267607032
openSNPrs267607032
23andMers267607032
23andMe allrs267607032
SNP Nexus

SNPshotrs267607032
SNPdbers267607032
MSV3drs267607032
GWAS Ctlgrs267607032
Max Magnitude0
ClinVar
Risk rs267607032(T;T)
Alt rs267607032(T;T)
Reference rs267607032(G;G)
Significance Pathogenic
Disease Paragangliomas 4 Hereditary cancer-predisposing syndrome not provided Paraganglioma and gastric stromal sarcoma Paragangliomas 1 Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Paragangliomas 4 Hereditary cancer-predisposing syndrome not provided Paraganglioma and gastric stromal sarcoma Paragangliomas 1 Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17355100C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013634.23, RCV000132167.2, RCV000183213.1, RCV000234325.1,