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rs1057516217

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516217(A;G)
Make rs1057516217(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position26193774
GeneGAREM2, HADHA, LOC107985860
is asnp
is mentioned by
dbSNPrs1057516217
dbSNP (old)rs1057516217
ClinGenrs1057516217
ebirs1057516217
HLIrs1057516217
Exacrs1057516217
Gnomadrs1057516217
Varsomers1057516217
Maprs1057516217
PheGenIrs1057516217
Biobankrs1057516217
1000 genomesrs1057516217
hgdprs1057516217
ensemblrs1057516217
gopubmedrs1057516217
geneviewrs1057516217
scholarrs1057516217
googlers1057516217
pharmgkbrs1057516217
gwascentralrs1057516217
openSNPrs1057516217
23andMers1057516217
23andMe allrs1057516217
SNPshotrs1057516217
SNPdbers1057516217
MSV3drs1057516217
GWAS Ctlgrs1057516217
Max Magnitude0
ClinVar
Risk rs1057516217(G;G)
Alt rs1057516217(G;G)
Reference Rs1057516217(A;A)
Significance Pathogenic
Disease Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency not provided
Variation info
Gene HADHA
CLNDBN Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency not provided
Reversed 1
HGVS NC_000002.11:g.26416643T>C
CLNSRC
CLNACC RCV000410623.1, RCV000439661.1,