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rs769580842

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs769580842(-;-)
Make rs769580842(-;AT)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position26193668
GeneGAREML, HADHA
is asnp
is mentioned by
dbSNPrs769580842
ebirs769580842
HLIrs769580842
Exacrs769580842
Varsomers769580842
Maprs769580842
PheGenIrs769580842
hapmaprs769580842
1000 genomesrs769580842
hgdprs769580842
ensemblrs769580842
gopubmedrs769580842
geneviewrs769580842
scholarrs769580842
googlers769580842
pharmgkbrs769580842
gwascentralrs769580842
openSNPrs769580842
23andMers769580842
23andMe allrs769580842
SNP Nexus

SNPshotrs769580842
SNPdbers769580842
MSV3drs769580842
GWAS Ctlgrs769580842
Max Magnitude0
ClinVar
Risk rs769580842(;)
Alt rs769580842(;)
Reference rs769580842(AT;AT)
Significance Probable-Pathogenic
Disease Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Variation info
Gene HADHA
CLNDBN Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Reversed 0
HGVS NC_000002.11:g.26416537_26416538delAT
CLNSRC
CLNACC RCV000169337.1,