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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
ebirs9370867
HLIrs9370867
Exacrs9370867
Varsomers9370867
Maprs9370867
PheGenIrs9370867
hapmaprs9370867
1000 genomesrs9370867
hgdprs9370867
ensemblrs9370867
gopubmedrs9370867
geneviewrs9370867
scholarrs9370867
googlers9370867
pharmgkbrs9370867
gwascentralrs9370867
openSNPrs9370867
23andMers9370867
23andMe allrs9370867
SNP Nexus

SNPshotrs9370867
SNPdbers9370867
MSV3drs9370867
GWAS Ctlgrs9370867
GMAF0.258
Max Magnitude
? (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


GET Evidence
MYLIP-N342S
aa_change Asn342Ser
aa_change_short N342S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.61675
summary



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