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rs17606561

From SNPedia

Orientationplus
Stabilizedplus
Make rs17606561(A;A)
Make rs17606561(A;G)
Make rs17606561(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10982126
GeneELOVL2
is asnp
is mentioned by
dbSNPrs17606561
dbSNP (classic)rs17606561
ClinGenrs17606561
ebirs17606561
HLIrs17606561
Exacrs17606561
Gnomadrs17606561
Varsomers17606561
LitVarrs17606561
Maprs17606561
PheGenIrs17606561
Biobankrs17606561
1000 genomesrs17606561
hgdprs17606561
ensemblrs17606561
geneviewrs17606561
scholarrs17606561
googlers17606561
pharmgkbrs17606561
gwascentralrs17606561
openSNPrs17606561
23andMers17606561
SNPshotrs17606561
SNPdbers17606561
MSV3drs17606561
GWAS Ctlgrs17606561
GMAF0.185
Max Magnitude0
? (A;A) (A;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 1E-11
Odds Ratio 0 None