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rs786205147

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205147(A;A)
Make rs786205147(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161340638
GeneSDHC
is asnp
is mentioned by
dbSNPrs786205147
ebirs786205147
HLIrs786205147
Exacrs786205147
Varsomers786205147
Maprs786205147
PheGenIrs786205147
hapmaprs786205147
1000 genomesrs786205147
hgdprs786205147
ensemblrs786205147
gopubmedrs786205147
geneviewrs786205147
scholarrs786205147
googlers786205147
pharmgkbrs786205147
gwascentralrs786205147
openSNPrs786205147
23andMers786205147
23andMe allrs786205147
SNP Nexus

SNPshotrs786205147
SNPdbers786205147
MSV3drs786205147
GWAS Ctlgrs786205147
Max Magnitude0
ClinVar
Risk rs786205147(A;A)
Alt rs786205147(A;A)
Reference rs786205147(G;G)
Significance Probable-Pathogenic
Disease Carney triad
Variation info
Gene SDHC
CLNDBN Carney triad
Reversed 0
HGVS NC_000001.10:g.161310428G>A
CLNSRC National Institutes of Health / The Eunice Kennedy Shriver National Institute of Child Health and Human Development
CLNACC RCV000170332.1,