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rs587776653

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776653(G;T)
Make rs587776653(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position161356841
GeneSDHC
is asnp
is mentioned by
dbSNPrs587776653
ebirs587776653
HLIrs587776653
Exacrs587776653
Varsomers587776653
Maprs587776653
PheGenIrs587776653
hapmaprs587776653
1000 genomesrs587776653
hgdprs587776653
ensemblrs587776653
gopubmedrs587776653
geneviewrs587776653
scholarrs587776653
googlers587776653
pharmgkbrs587776653
gwascentralrs587776653
openSNPrs587776653
23andMers587776653
23andMe allrs587776653
SNP Nexus

SNPshotrs587776653
SNPdbers587776653
MSV3drs587776653
GWAS Ctlgrs587776653
Max Magnitude0
ClinVar
Risk rs587776653(A,T;A,T)
Alt rs587776653(A,T;A,T)
Reference rs587776653(G;G)
Significance Pathogenic
Disease Paraganglioma and gastric stromal sarcoma Gastrointestinal stromal tumor Carney triad Paragangliomas 3
Variation info
Gene SDHC
CLNDBN Paraganglioma and gastric stromal sarcoma Gastrointestinal stromal tumor Carney triad Paragangliomas 3
Reversed 0
HGVS NC_000001.10:g.161326631G>A; NC_000001.10:g.161326631G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007666.3, RCV000023194.2, RCV000170333.1, RCV000007664.2,