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rs1137582

From SNPedia

Merged intors1135640
Orientationminus
Stabilizedminus
Make rs1137582(C;C)
Make rs1137582(C;G)
Make rs1137582(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position75953459
GeneACOX1
is asnp
is mentioned by
dbSNPrs1137582
ebirs1137582
HLIrs1137582
Exacrs1137582
Varsomers1137582
Maprs1137582
PheGenIrs1137582
hapmaprs1137582
1000 genomesrs1137582
hgdprs1137582
ensemblrs1137582
gopubmedrs1137582
geneviewrs1137582
scholarrs1137582
googlers1137582
pharmgkbrs1137582
gwascentralrs1137582
openSNPrs1137582
23andMers1137582
23andMe allrs1137582
SNP Nexus

SNPshotrs1137582
SNPdbers1137582
MSV3drs1137582
GWAS Ctlgrs1137582
StatusMerged into rs1135640
Max Magnitude
? (C;C) (C;G) (G;G) 28
Venter snp
Source plos
Gene ACOX1
allele C
frequency 0.65
sift
HuRef 1103645382811
Disease Association Defects in ACOX1 are the cause of pseudoneonatal adrenoleukodystrophy (MIM:264470). It is a disease biochemically characterized by an accumulation of very long chain fatty acids.