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rs587776644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776644(G;G)
Make rs587776644(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position112086961
GeneSDHD, TIMM8B
is asnp
is mentioned by
dbSNPrs587776644
ebirs587776644
HLIrs587776644
Exacrs587776644
Varsomers587776644
Maprs587776644
PheGenIrs587776644
hapmaprs587776644
1000 genomesrs587776644
hgdprs587776644
ensemblrs587776644
gopubmedrs587776644
geneviewrs587776644
scholarrs587776644
googlers587776644
pharmgkbrs587776644
gwascentralrs587776644
openSNPrs587776644
23andMers587776644
23andMe allrs587776644
SNP Nexus

SNPshotrs587776644
SNPdbers587776644
MSV3drs587776644
GWAS Ctlgrs587776644
Max Magnitude0
ClinVar
Risk rs587776644(G;G)
Alt rs587776644(G;G)
Reference rs587776644(T;T)
Significance Pathogenic
Disease Paragangliomas 1
Variation info
Gene TIMM8B SDHD
CLNDBN Paragangliomas 1
Reversed 0
HGVS NC_000011.9:g.111957685T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007298.2,