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rs786203932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786203932(A;A)
Make rs786203932(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position112094902
GeneSDHD
is asnp
is mentioned by
dbSNPrs786203932
dbSNP (classic)rs786203932
ClinGenrs786203932
ebirs786203932
HLIrs786203932
Exacrs786203932
Gnomadrs786203932
Varsomers786203932
LitVarrs786203932
Maprs786203932
PheGenIrs786203932
Biobankrs786203932
1000 genomesrs786203932
hgdprs786203932
ensemblrs786203932
geneviewrs786203932
scholarrs786203932
googlers786203932
pharmgkbrs786203932
gwascentralrs786203932
openSNPrs786203932
23andMers786203932
23andMe allrs786203932
SNPshotrs786203932
SNPdbers786203932
MSV3drs786203932
GWAS Ctlgrs786203932
Max Magnitude0
ClinVar
Risk rs786203932(A;A)
Alt rs786203932(A;A)
Reference Rs786203932(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene SDHD
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.111965626G>A
CLNSRC
CLNACC RCV000167450.2, RCV000478572.1,