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rs146036912

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs146036912(C;C)
Make rs146036912(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position108027727
GeneHADH
is asnp
is mentioned by
dbSNPrs146036912
ebirs146036912
HLIrs146036912
Exacrs146036912
Varsomers146036912
Maprs146036912
PheGenIrs146036912
hapmaprs146036912
1000 genomesrs146036912
hgdprs146036912
ensemblrs146036912
gopubmedrs146036912
geneviewrs146036912
scholarrs146036912
googlers146036912
pharmgkbrs146036912
gwascentralrs146036912
openSNPrs146036912
23andMers146036912
23andMe allrs146036912
SNP Nexus

SNPshotrs146036912
SNPdbers146036912
MSV3drs146036912
GWAS Ctlgrs146036912
Max Magnitude0
ClinVar
Risk rs146036912(C;C)
Alt rs146036912(C;C)
Reference rs146036912(T;T)
Significance Probable-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.108948883T>C
CLNSRC
CLNACC RCV000194052.1,