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rs770273135

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs770273135(C;C)
Make rs770273135(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position75745904
GeneACADM, DLSTP1
is asnp
is mentioned by
dbSNPrs770273135
ebirs770273135
HLIrs770273135
Exacrs770273135
Varsomers770273135
Maprs770273135
PheGenIrs770273135
hapmaprs770273135
1000 genomesrs770273135
hgdprs770273135
ensemblrs770273135
gopubmedrs770273135
geneviewrs770273135
scholarrs770273135
googlers770273135
pharmgkbrs770273135
gwascentralrs770273135
openSNPrs770273135
23andMers770273135
23andMe allrs770273135
SNP Nexus

SNPshotrs770273135
SNPdbers770273135
MSV3drs770273135
GWAS Ctlgrs770273135
Max Magnitude0
ClinVar
Risk rs770273135(A,C;A,C)
Alt rs770273135(A,C;A,C)
Reference rs770273135(T;T)
Significance Pathogenic
Disease not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency
Variation info
Gene DLSTP1 ACADM
CLNDBN not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.76211589T>C
CLNSRC
CLNACC RCV000185663.1, RCV000211549.1,