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rs786205436

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205436(A;G)
Make rs786205436(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position112088972
GeneSDHD
is asnp
is mentioned by
dbSNPrs786205436
ebirs786205436
HLIrs786205436
Exacrs786205436
Varsomers786205436
Maprs786205436
PheGenIrs786205436
hapmaprs786205436
1000 genomesrs786205436
hgdprs786205436
ensemblrs786205436
gopubmedrs786205436
geneviewrs786205436
scholarrs786205436
googlers786205436
pharmgkbrs786205436
gwascentralrs786205436
openSNPrs786205436
23andMers786205436
23andMe allrs786205436
SNP Nexus

SNPshotrs786205436
SNPdbers786205436
MSV3drs786205436
GWAS Ctlgrs786205436
Max Magnitude0
ClinVar
Risk rs786205436(G;G)
Alt rs786205436(G;G)
Reference rs786205436(A;A)
Significance Pathogenic
Disease Fatal infantile mitochondrial cardiomyopathy Mitochondrial complex II deficiency
Variation info
Gene SDHD
CLNDBN Fatal infantile mitochondrial cardiomyopathy Mitochondrial complex II deficiency
Reversed 0
HGVS NC_000011.9:g.111959696A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000171136.1, RCV000186596.2,