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rs1077989

From SNPedia

Orientationplus
Stabilizedplus
Make rs1077989(A;A)
Make rs1077989(A;C)
Make rs1077989(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position67509105
GeneTMEM229B
is asnp
is mentioned by
dbSNPrs1077989
ebirs1077989
HLIrs1077989
Exacrs1077989
Varsomers1077989
Maprs1077989
PheGenIrs1077989
hapmaprs1077989
1000 genomesrs1077989
hgdprs1077989
ensemblrs1077989
gopubmedrs1077989
geneviewrs1077989
scholarrs1077989
googlers1077989
pharmgkbrs1077989
gwascentralrs1077989
openSNPrs1077989
23andMers1077989
23andMe allrs1077989
SNP Nexus

SNPshotrs1077989
SNPdbers1077989
MSV3drs1077989
GWAS Ctlgrs1077989
GMAF0.3838
Max Magnitude
? (A;A) (A;C) (C;C) 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 9E-18
Odds Ratio 0 None