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rs137852768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852768(A;A)
Make rs137852768(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position251338
GeneSDHA
is asnp
is mentioned by
dbSNPrs137852768
ebirs137852768
HLIrs137852768
Exacrs137852768
Varsomers137852768
Maprs137852768
PheGenIrs137852768
hapmaprs137852768
1000 genomesrs137852768
hgdprs137852768
ensemblrs137852768
gopubmedrs137852768
geneviewrs137852768
scholarrs137852768
googlers137852768
pharmgkbrs137852768
gwascentralrs137852768
openSNPrs137852768
23andMers137852768
23andMe allrs137852768
SNP Nexus

SNPshotrs137852768
SNPdbers137852768
MSV3drs137852768
GWAS Ctlgrs137852768
Max Magnitude0
OMIM600857
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852768(A;A)
Alt rs137852768(A;A)
Reference rs137852768(G;G)
Significance Pathogenic
Disease Mitochondrial complex II deficiency Dilated cardiomyopathy 1GG
Variation info
Gene SDHA
CLNDBN Mitochondrial complex II deficiency Dilated cardiomyopathy 1GG
Reversed 0
HGVS NC_000005.9:g.251453G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009284.3, RCV000009286.3,