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rs786205209

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205209(C;C)
Make rs786205209(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position225434
GeneSDHA
is asnp
is mentioned by
dbSNPrs786205209
ebirs786205209
HLIrs786205209
Exacrs786205209
Varsomers786205209
Maprs786205209
PheGenIrs786205209
hapmaprs786205209
1000 genomesrs786205209
hgdprs786205209
ensemblrs786205209
gopubmedrs786205209
geneviewrs786205209
scholarrs786205209
googlers786205209
pharmgkbrs786205209
gwascentralrs786205209
openSNPrs786205209
23andMers786205209
23andMe allrs786205209
SNP Nexus

SNPshotrs786205209
SNPdbers786205209
MSV3drs786205209
GWAS Ctlgrs786205209
Max Magnitude0
ClinVar
Risk rs786205209(C;C)
Alt rs786205209(C;C)
Reference rs786205209(G;G)
Significance Probable-Pathogenic
Disease Mitochondrial complex II deficiency
Variation info
Gene SDHA
CLNDBN Mitochondrial complex II deficiency
Reversed 0
HGVS NC_000005.9:g.225549G>C
CLNSRC
CLNACC RCV000170440.1,