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rs786201085

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786201085(A;A)
Make rs786201085(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17022615
GeneSDHB
is asnp
is mentioned by
dbSNPrs786201085
ebirs786201085
HLIrs786201085
Exacrs786201085
Varsomers786201085
Maprs786201085
PheGenIrs786201085
hapmaprs786201085
1000 genomesrs786201085
hgdprs786201085
ensemblrs786201085
gopubmedrs786201085
geneviewrs786201085
scholarrs786201085
googlers786201085
pharmgkbrs786201085
gwascentralrs786201085
openSNPrs786201085
23andMers786201085
23andMe allrs786201085
SNP Nexus

SNPshotrs786201085
SNPdbers786201085
MSV3drs786201085
GWAS Ctlgrs786201085
Max Magnitude0
ClinVar
Risk rs786201085(A;A)
Alt rs786201085(A;A)
Reference rs786201085(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.17349110C>T
CLNSRC
CLNACC RCV000162580.1,