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rs786203457

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203457(A;G)
Make rs786203457(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161356815
GeneSDHC
is asnp
is mentioned by
dbSNPrs786203457
ebirs786203457
HLIrs786203457
Exacrs786203457
Varsomers786203457
Maprs786203457
PheGenIrs786203457
hapmaprs786203457
1000 genomesrs786203457
hgdprs786203457
ensemblrs786203457
gopubmedrs786203457
geneviewrs786203457
scholarrs786203457
googlers786203457
pharmgkbrs786203457
gwascentralrs786203457
openSNPrs786203457
23andMers786203457
23andMe allrs786203457
SNP Nexus

SNPshotrs786203457
SNPdbers786203457
MSV3drs786203457
GWAS Ctlgrs786203457
Max Magnitude0
ClinVar
Risk rs786203457(G;G)
Alt rs786203457(G;G)
Reference rs786203457(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000001.10:g.161326605A>G
CLNSRC
CLNACC RCV000166772.1,