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rs137852767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852767(C;T)
Make rs137852767(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position251011
GeneSDHA
is asnp
is mentioned by
dbSNPrs137852767
ebirs137852767
HLIrs137852767
Exacrs137852767
Varsomers137852767
Maprs137852767
PheGenIrs137852767
hapmaprs137852767
1000 genomesrs137852767
hgdprs137852767
ensemblrs137852767
gopubmedrs137852767
geneviewrs137852767
scholarrs137852767
googlers137852767
pharmgkbrs137852767
gwascentralrs137852767
openSNPrs137852767
23andMers137852767
23andMe allrs137852767
SNP Nexus

SNPshotrs137852767
SNPdbers137852767
MSV3drs137852767
GWAS Ctlgrs137852767
Max Magnitude0
OMIM600857
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852767(T;T)
Alt rs137852767(T;T)
Reference rs137852767(C;C)
Significance Pathogenic
Disease Mitochondrial complex II deficiency
Variation info
Gene SDHA
CLNDBN Mitochondrial complex II deficiency
Reversed 0
HGVS NC_000005.9:g.251126C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009282.3,