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rs864321638

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864321638(G;G)
Make rs864321638(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17033119
GeneSDHB
is asnp
is mentioned by
dbSNPrs864321638
ebirs864321638
HLIrs864321638
Exacrs864321638
Varsomers864321638
Maprs864321638
PheGenIrs864321638
hapmaprs864321638
1000 genomesrs864321638
hgdprs864321638
ensemblrs864321638
gopubmedrs864321638
geneviewrs864321638
scholarrs864321638
googlers864321638
pharmgkbrs864321638
gwascentralrs864321638
openSNPrs864321638
23andMers864321638
23andMe allrs864321638
SNP Nexus

SNPshotrs864321638
SNPdbers864321638
MSV3drs864321638
GWAS Ctlgrs864321638
Max Magnitude0
ClinVar
Risk rs864321638(G;G)
Alt rs864321638(G;G)
Reference rs864321638(T;T)
Significance Probable-Pathogenic
Disease Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17359614A>C
CLNSRC Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000203511.1,