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rs786205146

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205146(-;-)
Make rs786205146(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161314411
GeneSDHC
is asnp
is mentioned by
dbSNPrs786205146
ebirs786205146
HLIrs786205146
Exacrs786205146
Varsomers786205146
Maprs786205146
PheGenIrs786205146
hapmaprs786205146
1000 genomesrs786205146
hgdprs786205146
ensemblrs786205146
gopubmedrs786205146
geneviewrs786205146
scholarrs786205146
googlers786205146
pharmgkbrs786205146
gwascentralrs786205146
openSNPrs786205146
23andMers786205146
23andMe allrs786205146
SNP Nexus

SNPshotrs786205146
SNPdbers786205146
MSV3drs786205146
GWAS Ctlgrs786205146
Max Magnitude0
ClinVar
Risk rs786205146(;)
Alt rs786205146(;)
Reference rs786205146(T;T)
Significance Probable-Pathogenic
Disease Carney triad
Variation info
Gene SDHC
CLNDBN Carney triad
Reversed 0
HGVS NC_000001.10:g.161284201delT
CLNSRC National Institutes of Health / The Eunice Kennedy Shriver National Institute of Child Health and Human Development
CLNACC RCV000170331.1,