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rs9370867

From SNPedia

Orientationplus
Stabilizedplus
Make rs9370867(A;A)
Make rs9370867(A;G)
Make rs9370867(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position16145094
GeneMYLIP
is asnp
is mentioned by
dbSNPrs9370867
dbSNP (classic)rs9370867
ClinGenrs9370867
ebirs9370867
HLIrs9370867
Exacrs9370867
Gnomadrs9370867
Varsomers9370867
LitVarrs9370867
Maprs9370867
PheGenIrs9370867
Biobankrs9370867
1000 genomesrs9370867
hgdprs9370867
ensemblrs9370867
geneviewrs9370867
scholarrs9370867
googlers9370867
pharmgkbrs9370867
gwascentralrs9370867
openSNPrs9370867
23andMers9370867
SNPshotrs9370867
SNPdbers9370867
MSV3drs9370867
GWAS Ctlgrs9370867
GMAF0.258
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 21765216OA-icon.png] The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans


[PMID 25927920OA-icon.png] IDOL N342S Variant, Atherosclerosis Progression and Cardiovascular Disorders in the Italian General Population


[PMID 32868861OA-icon.png] IDOL gene variant is associated with hyperlipidemia in Han population in Xinjiang, China.