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rs4900442

From SNPedia

Orientationplus
Stabilizedplus
Make rs4900442(C;C)
Make rs4900442(C;T)
Make rs4900442(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position99691904
GeneCYP46A1
is asnp
is mentioned by
dbSNPrs4900442
ebirs4900442
HLIrs4900442
Exacrs4900442
Varsomers4900442
Maprs4900442
PheGenIrs4900442
hapmaprs4900442
1000 genomesrs4900442
hgdprs4900442
ensemblrs4900442
gopubmedrs4900442
geneviewrs4900442
scholarrs4900442
googlers4900442
pharmgkbrs4900442
gwascentralrs4900442
openSNPrs4900442
23andMers4900442
23andMe allrs4900442
SNP Nexus

SNPshotrs4900442
SNPdbers4900442
MSV3drs4900442
GWAS Ctlgrs4900442
GMAF0.4431
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19286353] CYP46A1 variants influence Alzheimer's disease risk and brain cholesterol metabolism


[PMID 16960449] Intron 2 (T/C) CYP46 polymorphism is associated with Alzheimer's disease in Chinese patients.