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rs587781720

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781720(C;T)
Make rs587781720(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position230923
GeneSDHA
is asnp
is mentioned by
dbSNPrs587781720
ebirs587781720
HLIrs587781720
Exacrs587781720
Varsomers587781720
Maprs587781720
PheGenIrs587781720
hapmaprs587781720
1000 genomesrs587781720
hgdprs587781720
ensemblrs587781720
gopubmedrs587781720
geneviewrs587781720
scholarrs587781720
googlers587781720
pharmgkbrs587781720
gwascentralrs587781720
openSNPrs587781720
23andMers587781720
23andMe allrs587781720
SNP Nexus

SNPshotrs587781720
SNPdbers587781720
MSV3drs587781720
GWAS Ctlgrs587781720
Max Magnitude0
ClinVar
Risk rs587781720(T;T)
Alt rs587781720(T;T)
Reference rs587781720(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHA
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.231038C>T
CLNSRC
CLNACC RCV000129906.2,