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rs766667009

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766667009(G;T)
Make rs766667009(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position251104
GeneSDHA
is asnp
is mentioned by
dbSNPrs766667009
dbSNP (old)rs766667009
ClinGenrs766667009
ebirs766667009
HLIrs766667009
Exacrs766667009
Varsomers766667009
Maprs766667009
PheGenIrs766667009
Biobankrs766667009
1000 genomesrs766667009
hgdprs766667009
ensemblrs766667009
gopubmedrs766667009
geneviewrs766667009
scholarrs766667009
googlers766667009
pharmgkbrs766667009
gwascentralrs766667009
openSNPrs766667009
23andMers766667009
23andMe allrs766667009
SNP Nexus

SNPshotrs766667009
SNPdbers766667009
MSV3drs766667009
GWAS Ctlgrs766667009
Max Magnitude0
ClinVar
Risk rs766667009(T;T)
Alt rs766667009(T;T)
Reference Rs766667009(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Mitochondrial complex II deficiency Paragangliomas 5
Variation info
Gene SDHA
CLNDBN Hereditary cancer-predisposing syndrome Mitochondrial complex II deficiency Paragangliomas 5
Reversed 0
HGVS NC_000005.9:g.251219G>T
CLNSRC
CLNACC RCV000218973.1, RCV000466792.1,