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rs587781266

From SNPedia

Orientationminus
Geno Mag Summary
(CTCT;CTCT) 0 common in clinvar
Make rs587781266(-;-)
Make rs587781266(-;CTCT)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position17022654
GeneSDHB
is asnp
is mentioned by
dbSNPrs587781266
ebirs587781266
HLIrs587781266
Exacrs587781266
Varsomers587781266
Maprs587781266
PheGenIrs587781266
hapmaprs587781266
1000 genomesrs587781266
hgdprs587781266
ensemblrs587781266
gopubmedrs587781266
geneviewrs587781266
scholarrs587781266
googlers587781266
pharmgkbrs587781266
gwascentralrs587781266
openSNPrs587781266
23andMers587781266
23andMe allrs587781266
SNP Nexus

SNPshotrs587781266
SNPdbers587781266
MSV3drs587781266
GWAS Ctlgrs587781266
Max Magnitude0
ClinVar
Risk rs587781266(;)
Alt rs587781266(;)
Reference rs587781266(CTCT;CTCT)
Significance Pathogenic
Disease Paragangliomas 4 Pheochromocytoma Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Paragangliomas 4 Pheochromocytoma Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17349149_17349152delAGAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000013621.23, RCV000013622.23, RCV000128877.2,