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rs397514541

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514541(C;T)
Make rs397514541(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position240451
GeneSDHA
is asnp
is mentioned by
dbSNPrs397514541
ebirs397514541
HLIrs397514541
Exacrs397514541
Varsomers397514541
Maprs397514541
PheGenIrs397514541
hapmaprs397514541
1000 genomesrs397514541
hgdprs397514541
ensemblrs397514541
gopubmedrs397514541
geneviewrs397514541
scholarrs397514541
googlers397514541
pharmgkbrs397514541
gwascentralrs397514541
openSNPrs397514541
23andMers397514541
23andMe allrs397514541
SNP Nexus

SNPshotrs397514541
SNPdbers397514541
MSV3drs397514541
GWAS Ctlgrs397514541
Max Magnitude0
ClinVar
Risk rs397514541(T;T)
Alt rs397514541(T;T)
Reference rs397514541(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.240566C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032786.4,