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rs786201063

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786201063(A;A)
Make rs786201063(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17033059
GeneSDHB
is asnp
is mentioned by
dbSNPrs786201063
ebirs786201063
HLIrs786201063
Exacrs786201063
Varsomers786201063
Maprs786201063
PheGenIrs786201063
hapmaprs786201063
1000 genomesrs786201063
hgdprs786201063
ensemblrs786201063
gopubmedrs786201063
geneviewrs786201063
scholarrs786201063
googlers786201063
pharmgkbrs786201063
gwascentralrs786201063
openSNPrs786201063
23andMers786201063
23andMe allrs786201063
SNP Nexus

SNPshotrs786201063
SNPdbers786201063
MSV3drs786201063
GWAS Ctlgrs786201063
Max Magnitude0
ClinVar
Risk rs786201063(A;A)
Alt rs786201063(A;A)
Reference rs786201063(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17359554C>T
CLNSRC
CLNACC RCV000162475.1,