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rs3829462

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(T;T) 0 common in complete genomics
Make rs3829462(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position58560880
GeneLIPC
is asnp
is mentioned by
dbSNPrs3829462
dbSNP (old)rs3829462
ClinGenrs3829462
ebirs3829462
HLIrs3829462
Exacrs3829462
Gnomadrs3829462
Varsomers3829462
Maprs3829462
PheGenIrs3829462
Biobankrs3829462
1000 genomesrs3829462
hgdprs3829462
ensemblrs3829462
gopubmedrs3829462
geneviewrs3829462
scholarrs3829462
googlers3829462
pharmgkbrs3829462
gwascentralrs3829462
openSNPrs3829462
23andMers3829462
23andMe allrs3829462
SNPshotrs3829462
SNPdbers3829462
MSV3drs3829462
GWAS Ctlgrs3829462
GMAF0.06979
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[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.



ClinVar
Risk Rs3829462(T;T)
Alt Rs3829462(T;T)
Reference Rs3829462(G;G)
Significance Non-pathogenic
Disease Hepatic lipase deficiency
Variation info
Gene LIPC
CLNDBN Hepatic lipase deficiency
Reversed 1
HGVS NC_000015.9:g.58853079C>A
CLNSRC
CLNACC RCV000382130.1,