Have questions? Visit https://www.reddit.com/r/SNPedia

rs587782617

From SNPedia

Orientationminus
Geno Mag Summary
(GGAGACAAAT;GGAGACAAAT) 0 common in clinvar
Make rs587782617(-;-)
Make rs587782617(-;GGAGACAAAT)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position17023999
GeneSDHB
is asnp
is mentioned by
dbSNPrs587782617
ebirs587782617
HLIrs587782617
Exacrs587782617
Varsomers587782617
Maprs587782617
PheGenIrs587782617
hapmaprs587782617
1000 genomesrs587782617
hgdprs587782617
ensemblrs587782617
gopubmedrs587782617
geneviewrs587782617
scholarrs587782617
googlers587782617
pharmgkbrs587782617
gwascentralrs587782617
openSNPrs587782617
23andMers587782617
23andMe allrs587782617
SNP Nexus

SNPshotrs587782617
SNPdbers587782617
MSV3drs587782617
GWAS Ctlgrs587782617
Max Magnitude0
ClinVar
Risk rs587782617(;)
Alt rs587782617(;)
Reference rs587782617(GGAGACAAAT;GGAGACAAAT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17350494_17350503delATTTGTCTCC
CLNSRC
CLNACC RCV000131995.2,