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rs17718828

From SNPedia

Orientationplus
Stabilizedplus
Make rs17718828(C;C)
Make rs17718828(C;T)
Make rs17718828(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position74553977
GeneLINC00347
is asnp
is mentioned by
dbSNPrs17718828
ebirs17718828
HLIrs17718828
Exacrs17718828
Varsomers17718828
Maprs17718828
PheGenIrs17718828
hapmaprs17718828
1000 genomesrs17718828
hgdprs17718828
ensemblrs17718828
gopubmedrs17718828
geneviewrs17718828
scholarrs17718828
googlers17718828
pharmgkbrs17718828
gwascentralrs17718828
openSNPrs17718828
23andMers17718828
23andMe allrs17718828
SNP Nexus

SNPshotrs17718828
SNPdbers17718828
MSV3drs17718828
GWAS Ctlgrs17718828
GMAF0.06152
Max Magnitude
? (C;C) (C;T) (T;T) 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 1E-8
Odds Ratio 0.8000 None