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rs4666002

From SNPedia

Orientationplus
Stabilizedplus
Make rs4666002(C;C)
Make rs4666002(C;G)
Make rs4666002(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position27617773
GeneZNF512
is asnp
is mentioned by
dbSNPrs4666002
ebirs4666002
HLIrs4666002
Exacrs4666002
Varsomers4666002
Maprs4666002
PheGenIrs4666002
hapmaprs4666002
1000 genomesrs4666002
hgdprs4666002
ensemblrs4666002
gopubmedrs4666002
geneviewrs4666002
scholarrs4666002
googlers4666002
pharmgkbrs4666002
gwascentralrs4666002
openSNPrs4666002
23andMers4666002
23andMe allrs4666002
SNP Nexus

SNPshotrs4666002
SNPdbers4666002
MSV3drs4666002
GWAS Ctlgrs4666002
GMAF0.3264
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22359512OA-icon.png]
Trait
Title Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
Risk Allele
P-val 7E-11
Odds Ratio 0 None