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rs9809219

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9809219(C;T)
Make rs9809219(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position251100
GeneSDHA
is asnp
is mentioned by
dbSNPrs9809219
ebirs9809219
HLIrs9809219
Exacrs9809219
Varsomers9809219
Maprs9809219
PheGenIrs9809219
hapmaprs9809219
1000 genomesrs9809219
hgdprs9809219
ensemblrs9809219
gopubmedrs9809219
geneviewrs9809219
scholarrs9809219
googlers9809219
pharmgkbrs9809219
gwascentralrs9809219
openSNPrs9809219
23andMers9809219
23andMe allrs9809219
SNP Nexus

SNPshotrs9809219
SNPdbers9809219
MSV3drs9809219
GWAS Ctlgrs9809219
Max Magnitude0
OMIM600857
Desc
Variant0001
Relatedalso
ClinVar
Risk rs9809219(T;T)
Alt rs9809219(T;T)
Reference rs9809219(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.251215C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009281.3,