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rs786201161

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786201161(A;G)
Make rs786201161(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17024076
GeneSDHB
is asnp
is mentioned by
dbSNPrs786201161
ebirs786201161
HLIrs786201161
Exacrs786201161
Varsomers786201161
Maprs786201161
PheGenIrs786201161
hapmaprs786201161
1000 genomesrs786201161
hgdprs786201161
ensemblrs786201161
gopubmedrs786201161
geneviewrs786201161
scholarrs786201161
googlers786201161
pharmgkbrs786201161
gwascentralrs786201161
openSNPrs786201161
23andMers786201161
23andMe allrs786201161
SNP Nexus

SNPshotrs786201161
SNPdbers786201161
MSV3drs786201161
GWAS Ctlgrs786201161
Max Magnitude0
ClinVar
Risk rs786201161(G;G)
Alt rs786201161(G;G)
Reference rs786201161(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17350571T>C
CLNSRC
CLNACC RCV000162804.1,