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rs794727700

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727700(A;G)
Make rs794727700(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position26234267
GeneHADHA
is asnp
is mentioned by
dbSNPrs794727700
ebirs794727700
HLIrs794727700
Exacrs794727700
Varsomers794727700
Maprs794727700
PheGenIrs794727700
hapmaprs794727700
1000 genomesrs794727700
hgdprs794727700
ensemblrs794727700
gopubmedrs794727700
geneviewrs794727700
scholarrs794727700
googlers794727700
pharmgkbrs794727700
gwascentralrs794727700
openSNPrs794727700
23andMers794727700
23andMe allrs794727700
SNP Nexus

SNPshotrs794727700
SNPdbers794727700
MSV3drs794727700
GWAS Ctlgrs794727700
Max Magnitude0
ClinVar
Risk rs794727700(G;G)
Alt rs794727700(G;G)
Reference rs794727700(A;A)
Significance Probable-Pathogenic
Disease Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Variation info
Gene HADHA
CLNDBN Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Reversed 1
HGVS NC_000002.11:g.26457135T>C
CLNSRC
CLNACC RCV000178729.1,