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rs587778661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778661(C;T)
Make rs587778661(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position161328466
GeneSDHC
is asnp
is mentioned by
dbSNPrs587778661
dbSNP (classic)rs587778661
ClinGenrs587778661
ebirs587778661
HLIrs587778661
Exacrs587778661
Gnomadrs587778661
Varsomers587778661
LitVarrs587778661
Maprs587778661
PheGenIrs587778661
Biobankrs587778661
1000 genomesrs587778661
hgdprs587778661
ensemblrs587778661
geneviewrs587778661
scholarrs587778661
googlers587778661
pharmgkbrs587778661
gwascentralrs587778661
openSNPrs587778661
23andMers587778661
23andMe allrs587778661
SNPshotrs587778661
SNPdbers587778661
MSV3drs587778661
GWAS Ctlgrs587778661
Max Magnitude0
ClinVar
Risk rs587778661(T;T)
Alt rs587778661(T;T)
Reference Rs587778661(C;C)
Significance Probable-Pathogenic
Disease not specified Hereditary cancer-predisposing syndrome
Variation info
Gene SDHC
CLNDBN not specified Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000001.10:g.161298256C>T
CLNSRC
CLNACC RCV000122003.1, RCV000492504.1,