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rs137853101

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853101(A;A)
Make rs137853101(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position107990050
GeneHADH
is asnp
is mentioned by
dbSNPrs137853101
ebirs137853101
HLIrs137853101
Exacrs137853101
Varsomers137853101
Maprs137853101
PheGenIrs137853101
hapmaprs137853101
1000 genomesrs137853101
hgdprs137853101
ensemblrs137853101
gopubmedrs137853101
geneviewrs137853101
scholarrs137853101
googlers137853101
pharmgkbrs137853101
gwascentralrs137853101
openSNPrs137853101
23andMers137853101
23andMe allrs137853101
SNP Nexus

SNPshotrs137853101
SNPdbers137853101
MSV3drs137853101
GWAS Ctlgrs137853101
Max Magnitude0
OMIM601609
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853101(A;A)
Alt rs137853101(A;A)
Reference rs137853101(G;G)
Significance Pathogenic
Disease Deficiency of 3-hydroxyacyl-CoA dehydrogenase
Variation info
Gene HADH
CLNDBN Deficiency of 3-hydroxyacyl-CoA dehydrogenase
Reversed 0
HGVS NC_000004.11:g.108911206G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008482.1,