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rs786202732

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786202732(C;C)
Make rs786202732(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17024041
GeneSDHB
is asnp
is mentioned by
dbSNPrs786202732
ebirs786202732
HLIrs786202732
Exacrs786202732
Varsomers786202732
Maprs786202732
PheGenIrs786202732
hapmaprs786202732
1000 genomesrs786202732
hgdprs786202732
ensemblrs786202732
gopubmedrs786202732
geneviewrs786202732
scholarrs786202732
googlers786202732
pharmgkbrs786202732
gwascentralrs786202732
openSNPrs786202732
23andMers786202732
23andMe allrs786202732
SNP Nexus

SNPshotrs786202732
SNPdbers786202732
MSV3drs786202732
GWAS Ctlgrs786202732
Max Magnitude0
ClinVar
Risk rs786202732(C;C)
Alt rs786202732(C;C)
Reference rs786202732(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17350536A>G
CLNSRC
CLNACC RCV000165688.1,