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rs587782904

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782904(A;A)
Make rs587782904(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position17033143
GeneSDHB
is asnp
is mentioned by
dbSNPrs587782904
ClinGenrs587782904
ebirs587782904
HLIrs587782904
Exacrs587782904
Varsomers587782904
Maprs587782904
PheGenIrs587782904
hapmaprs587782904
1000 genomesrs587782904
hgdprs587782904
ensemblrs587782904
gopubmedrs587782904
geneviewrs587782904
scholarrs587782904
googlers587782904
pharmgkbrs587782904
gwascentralrs587782904
openSNPrs587782904
23andMers587782904
23andMe allrs587782904
SNP Nexus

SNPshotrs587782904
SNPdbers587782904
MSV3drs587782904
GWAS Ctlgrs587782904
Max Magnitude0
ClinVar
Risk rs587782904(A;A)
Alt rs587782904(A;A)
Reference Rs587782904(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17359638C>T
CLNSRC
CLNACC RCV000132547.2,