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rs3829462

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs3829462(G;G)
Make rs3829462(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position58560880
GeneLIPC
is asnp
is mentioned by
dbSNPrs3829462
ebirs3829462
HLIrs3829462
Exacrs3829462
Varsomers3829462
Maprs3829462
PheGenIrs3829462
hapmaprs3829462
1000 genomesrs3829462
hgdprs3829462
ensemblrs3829462
gopubmedrs3829462
geneviewrs3829462
scholarrs3829462
googlers3829462
pharmgkbrs3829462
gwascentralrs3829462
openSNPrs3829462
23andMers3829462
23andMe allrs3829462
SNP Nexus

SNPshotrs3829462
SNPdbers3829462
MSV3drs3829462
GWAS Ctlgrs3829462
GMAF0.06979
Max Magnitude0
? (G;G) (G;T) (T;T) 28


Venter snp
Source plos
Gene LIPC
allele A
frequency 0.025
sift
HuRef 1103645624063
Disease Association Defects in LIPC are the cause of hepatic lipase deficiency (HL deficiency) (MIM:151670).



[PMID 17903301OA-icon.png] Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.

[PMID 19041386OA-icon.png] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.


GET Evidence
LIPC-F356L
aa_change Phe356Leu
aa_change_short F356L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.946458
summary