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rs202198133

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202198133(A;A)
Make rs202198133(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position112088902
GeneSDHD
is asnp
is mentioned by
dbSNPrs202198133
ebirs202198133
HLIrs202198133
Exacrs202198133
Varsomers202198133
Maprs202198133
PheGenIrs202198133
hapmaprs202198133
1000 genomesrs202198133
hgdprs202198133
ensemblrs202198133
gopubmedrs202198133
geneviewrs202198133
scholarrs202198133
googlers202198133
pharmgkbrs202198133
gwascentralrs202198133
openSNPrs202198133
23andMers202198133
23andMe allrs202198133
SNP Nexus

SNPshotrs202198133
SNPdbers202198133
MSV3drs202198133
GWAS Ctlgrs202198133
Max Magnitude0
ClinVar
Risk rs202198133(A;A)
Alt rs202198133(A;A)
Reference rs202198133(G;G)
Significance Pathogenic
Disease Mitochondrial complex II deficiency
Variation info
Gene SDHD
CLNDBN Mitochondrial complex II deficiency
Reversed 0
HGVS NC_000011.9:g.111959626G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144171.3,