Have questions? Visit https://www.reddit.com/r/SNPedia

rs137853102

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853102(A;A)
Make rs137853102(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position108009797
GeneHADH
is asnp
is mentioned by
dbSNPrs137853102
ebirs137853102
HLIrs137853102
Exacrs137853102
Varsomers137853102
Maprs137853102
PheGenIrs137853102
hapmaprs137853102
1000 genomesrs137853102
hgdprs137853102
ensemblrs137853102
gopubmedrs137853102
geneviewrs137853102
scholarrs137853102
googlers137853102
pharmgkbrs137853102
gwascentralrs137853102
openSNPrs137853102
23andMers137853102
23andMe allrs137853102
SNP Nexus

SNPshotrs137853102
SNPdbers137853102
MSV3drs137853102
GWAS Ctlgrs137853102
Max Magnitude0
OMIM601609
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853102(A;A)
Alt rs137853102(A;A)
Reference rs137853102(C;C)
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.108930953C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008483.2,