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rs587782210

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782210(A;A)
Make rs587782210(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position112087959
GeneSDHD, TIMM8B
is asnp
is mentioned by
dbSNPrs587782210
ebirs587782210
HLIrs587782210
Exacrs587782210
Varsomers587782210
Maprs587782210
PheGenIrs587782210
hapmaprs587782210
1000 genomesrs587782210
hgdprs587782210
ensemblrs587782210
gopubmedrs587782210
geneviewrs587782210
scholarrs587782210
googlers587782210
pharmgkbrs587782210
gwascentralrs587782210
openSNPrs587782210
23andMers587782210
23andMe allrs587782210
SNP Nexus

SNPshotrs587782210
SNPdbers587782210
MSV3drs587782210
GWAS Ctlgrs587782210
Max Magnitude0
ClinVar
Risk rs587782210(A;A)
Alt rs587782210(A;A)
Reference rs587782210(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TIMM8B SDHD
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.111958683C>A
CLNSRC
CLNACC RCV000130886.2,