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rs11246602

From SNPedia

Orientationminus
Stabilizedminus
Make rs11246602(C;C)
Make rs11246602(C;T)
Make rs11246602(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position54607190
is asnp
is mentioned by
dbSNPrs11246602
ebirs11246602
HLIrs11246602
Exacrs11246602
Varsomers11246602
Maprs11246602
PheGenIrs11246602
hapmaprs11246602
1000 genomesrs11246602
hgdprs11246602
ensemblrs11246602
gopubmedrs11246602
geneviewrs11246602
scholarrs11246602
googlers11246602
pharmgkbrs11246602
gwascentralrs11246602
openSNPrs11246602
23andMers11246602
23andMe allrs11246602
SNP Nexus

SNPshotrs11246602
SNPdbers11246602
MSV3drs11246602
GWAS Ctlgrs11246602
Max Magnitude
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait HDL cholesterol
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele C
P-val 2E-10
Odds Ratio .03 [NR] unit increase