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rs864321636

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864321636(C;C)
Make rs864321636(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17028685
GeneSDHB
is asnp
is mentioned by
dbSNPrs864321636
ebirs864321636
HLIrs864321636
Exacrs864321636
Varsomers864321636
Maprs864321636
PheGenIrs864321636
hapmaprs864321636
1000 genomesrs864321636
hgdprs864321636
ensemblrs864321636
gopubmedrs864321636
geneviewrs864321636
scholarrs864321636
googlers864321636
pharmgkbrs864321636
gwascentralrs864321636
openSNPrs864321636
23andMers864321636
23andMe allrs864321636
SNP Nexus

SNPshotrs864321636
SNPdbers864321636
MSV3drs864321636
GWAS Ctlgrs864321636
Max Magnitude0
ClinVar
Risk rs864321636(C;C)
Alt rs864321636(C;C)
Reference rs864321636(G;G)
Significance Probable-Pathogenic
Disease Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17355180C>G
CLNSRC Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000203531.1,