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rs786201095

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786201095(G;G)
Make rs786201095(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17028643
GeneSDHB
is asnp
is mentioned by
dbSNPrs786201095
ebirs786201095
HLIrs786201095
Exacrs786201095
Varsomers786201095
Maprs786201095
PheGenIrs786201095
hapmaprs786201095
1000 genomesrs786201095
hgdprs786201095
ensemblrs786201095
gopubmedrs786201095
geneviewrs786201095
scholarrs786201095
googlers786201095
pharmgkbrs786201095
gwascentralrs786201095
openSNPrs786201095
23andMers786201095
23andMe allrs786201095
SNP Nexus

SNPshotrs786201095
SNPdbers786201095
MSV3drs786201095
GWAS Ctlgrs786201095
Max Magnitude0
ClinVar
Risk rs786201095(G;G)
Alt rs786201095(G;G)
Reference rs786201095(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Carney triad not provided
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome Carney triad not provided
Reversed 1
HGVS NC_000001.10:g.17355138A>C
CLNSRC National Institutes of Health / The Eunice Kennedy Shriver National Institute of Child Health and Human Development
CLNACC RCV000162628.1, RCV000170330.1, RCV000183212.1,