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rs151266052

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151266052(C;T)
Make rs151266052(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position240448
GeneSDHA
is asnp
is mentioned by
dbSNPrs151266052
ebirs151266052
HLIrs151266052
Exacrs151266052
Varsomers151266052
Maprs151266052
PheGenIrs151266052
hapmaprs151266052
1000 genomesrs151266052
hgdprs151266052
ensemblrs151266052
gopubmedrs151266052
geneviewrs151266052
scholarrs151266052
googlers151266052
pharmgkbrs151266052
gwascentralrs151266052
openSNPrs151266052
23andMers151266052
23andMe allrs151266052
SNP Nexus

SNPshotrs151266052
SNPdbers151266052
MSV3drs151266052
GWAS Ctlgrs151266052
GMAF0.003214
Max Magnitude0
ClinVar
Risk rs151266052(T;T)
Alt rs151266052(T;T)
Reference rs151266052(C;C)
Significance Pathogenic
Disease Mitochondrial complex II deficiency Paragangliomas 5
Variation info
Gene SDHA
CLNDBN Mitochondrial complex II deficiency Paragangliomas 5
Reversed 0
HGVS NC_000005.9:g.240563C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032785.2, RCV000232220.1,