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rs4986970

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs4986970(A;A)
Make rs4986970(A;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position67942417
GeneLCAT
is asnp
is mentioned by
dbSNPrs4986970
ebirs4986970
HLIrs4986970
Exacrs4986970
Varsomers4986970
Maprs4986970
PheGenIrs4986970
hapmaprs4986970
1000 genomesrs4986970
hgdprs4986970
ensemblrs4986970
gopubmedrs4986970
geneviewrs4986970
scholarrs4986970
googlers4986970
pharmgkbrs4986970
gwascentralrs4986970
openSNPrs4986970
23andMers4986970
23andMe allrs4986970
SNP Nexus

SNPshotrs4986970
SNPdbers4986970
MSV3drs4986970
GWAS Ctlgrs4986970
GMAF0.01148
Max Magnitude0
? (A;A) (A;T) (T;T) 28

[PMID 22090275] LCAT, HDL Cholesterol and Ischemic Cardiovascular Disease: A Mendelian Randomization Study of HDL Cholesterol in 54,500 Individuals


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


[PMID 19408013OA-icon.png] Strategies and issues in the detection of pathway enrichment in genome-wide association studies.


GET Evidence
LCAT-S232T
aa_change Ser232Thr
aa_change_short S232T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0230526
summary



[PMID 24789697] Identification of genetic variants of lecithin cholesterol acyltransferase in individuals with high HDL‑C levels