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rs864321637

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864321637(A;C)
Make rs864321637(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17033095
GeneSDHB
is asnp
is mentioned by
dbSNPrs864321637
ebirs864321637
HLIrs864321637
Exacrs864321637
Varsomers864321637
Maprs864321637
PheGenIrs864321637
hapmaprs864321637
1000 genomesrs864321637
hgdprs864321637
ensemblrs864321637
gopubmedrs864321637
geneviewrs864321637
scholarrs864321637
googlers864321637
pharmgkbrs864321637
gwascentralrs864321637
openSNPrs864321637
23andMers864321637
23andMe allrs864321637
SNP Nexus

SNPshotrs864321637
SNPdbers864321637
MSV3drs864321637
GWAS Ctlgrs864321637
Max Magnitude0
ClinVar
Risk rs864321637(C;C)
Alt rs864321637(C;C)
Reference rs864321637(A;A)
Significance Probable-Pathogenic
Disease Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17359590T>G
CLNSRC Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000203547.1,