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rs1057516461

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516461(A;T)
Make rs1057516461(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position26201304
GeneGAREM2, HADHA
is asnp
is mentioned by
dbSNPrs1057516461
dbSNP (old)rs1057516461
ClinGenrs1057516461
ebirs1057516461
HLIrs1057516461
Exacrs1057516461
Gnomadrs1057516461
Varsomers1057516461
Maprs1057516461
PheGenIrs1057516461
Biobankrs1057516461
1000 genomesrs1057516461
hgdprs1057516461
ensemblrs1057516461
gopubmedrs1057516461
geneviewrs1057516461
scholarrs1057516461
googlers1057516461
pharmgkbrs1057516461
gwascentralrs1057516461
openSNPrs1057516461
23andMers1057516461
23andMe allrs1057516461
SNPshotrs1057516461
SNPdbers1057516461
MSV3drs1057516461
GWAS Ctlgrs1057516461
Max Magnitude0
ClinVar
Risk rs1057516461(T;T)
Alt rs1057516461(T;T)
Reference Rs1057516461(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.26424173T>A
CLNSRC
CLNACC RCV000410271.1,