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rs1529729

From SNPedia

Orientationminus
Stabilizedminus
Make rs1529729(A;A)
Make rs1529729(A;G)
Make rs1529729(G;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position11052886
GeneSMARCA4
is asnp
is mentioned by
dbSNPrs1529729
dbSNP (classic)rs1529729
ClinGenrs1529729
ebirs1529729
HLIrs1529729
Exacrs1529729
Gnomadrs1529729
Varsomers1529729
LitVarrs1529729
Maprs1529729
PheGenIrs1529729
Biobankrs1529729
1000 genomesrs1529729
hgdprs1529729
ensemblrs1529729
geneviewrs1529729
scholarrs1529729
googlers1529729
pharmgkbrs1529729
gwascentralrs1529729
openSNPrs1529729
23andMers1529729
SNPshotrs1529729
SNPdbers1529729
MSV3drs1529729
GWAS Ctlgrs1529729
GMAF0.3866
Max Magnitude0
? (A;A) (A;G) (G;G) 28


OMIM606945
DescLOW DENSITY LIPOPROTEIN RECEPTOR; LDLR
Variant
Relatedalso


[PMID 19773416OA-icon.png] A gene score of nine LDL and HDL regulating genes is associated with fluvastatin-induced cholesterol changes in women


[PMID 18714375OA-icon.png] Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study.


[PMID 19913121OA-icon.png] Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.


[PMID 19951432OA-icon.png] Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.