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rs267606859

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606859(G;G)
Make rs267606859(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26285546
GeneHADHB
is asnp
is mentioned by
dbSNPrs267606859
ebirs267606859
HLIrs267606859
Exacrs267606859
Varsomers267606859
Maprs267606859
PheGenIrs267606859
hapmaprs267606859
1000 genomesrs267606859
hgdprs267606859
ensemblrs267606859
gopubmedrs267606859
geneviewrs267606859
scholarrs267606859
googlers267606859
pharmgkbrs267606859
gwascentralrs267606859
openSNPrs267606859
23andMers267606859
23andMe allrs267606859
SNP Nexus

SNPshotrs267606859
SNPdbers267606859
MSV3drs267606859
GWAS Ctlgrs267606859
Max Magnitude0
ClinVar
Risk rs267606859(A,C,G;A,C,G)
Alt rs267606859(A,C,G;A,C,G)
Reference rs267606859(T;T)
Significance Pathogenic
Disease Mitochondrial trifunctional protein deficiency
Variation info
Gene HADHB
CLNDBN Mitochondrial trifunctional protein deficiency
Reversed 0
HGVS NC_000002.11:g.26508414T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015974.28,