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rs779113356

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs779113356(-;-)
Make rs779113356(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position26192343
GeneGAREM2, HADHA, LOC107985860
is asnp
is mentioned by
dbSNPrs779113356
dbSNP (old)rs779113356
ClinGenrs779113356
ebirs779113356
HLIrs779113356
Exacrs779113356
Varsomers779113356
Maprs779113356
PheGenIrs779113356
Biobankrs779113356
1000 genomesrs779113356
hgdprs779113356
ensemblrs779113356
gopubmedrs779113356
geneviewrs779113356
scholarrs779113356
googlers779113356
pharmgkbrs779113356
gwascentralrs779113356
openSNPrs779113356
23andMers779113356
23andMe allrs779113356
SNP Nexus

SNPshotrs779113356
SNPdbers779113356
MSV3drs779113356
GWAS Ctlgrs779113356
Max Magnitude0
ClinVar
Risk rs779113356(-;-)
Alt rs779113356(-;-)
Reference Rs779113356(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 0
HGVS NC_000002.11:g.26415212delA
CLNSRC
CLNACC RCV000169001.1, RCV000255407.1,