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rs1250229

From SNPedia

Orientationplus
Stabilizedplus
Make rs1250229(C;C)
Make rs1250229(C;T)
Make rs1250229(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position215439661
is asnp
is mentioned by
dbSNPrs1250229
dbSNP (classic)rs1250229
ClinGenrs1250229
ebirs1250229
HLIrs1250229
Exacrs1250229
Gnomadrs1250229
Varsomers1250229
LitVarrs1250229
Maprs1250229
PheGenIrs1250229
Biobankrs1250229
1000 genomesrs1250229
hgdprs1250229
ensemblrs1250229
geneviewrs1250229
scholarrs1250229
googlers1250229
pharmgkbrs1250229
gwascentralrs1250229
openSNPrs1250229
23andMers1250229
SNPshotrs1250229
SNPdbers1250229
MSV3drs1250229
GWAS Ctlgrs1250229
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait LDL cholesterol
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele T
P-val 3E-8
Odds Ratio .02 [NR] unit decrease