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rs9832727

From SNPedia

Orientationplus
Stabilizedplus
Make rs9832727(C;C)
Make rs9832727(C;G)
Make rs9832727(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position142930268
GeneLOC100507389
is asnp
is mentioned by
dbSNPrs9832727
dbSNP (classic)rs9832727
ClinGenrs9832727
ebirs9832727
HLIrs9832727
Exacrs9832727
Gnomadrs9832727
Varsomers9832727
LitVarrs9832727
Maprs9832727
PheGenIrs9832727
Biobankrs9832727
1000 genomesrs9832727
hgdprs9832727
ensemblrs9832727
geneviewrs9832727
scholarrs9832727
googlers9832727
pharmgkbrs9832727
gwascentralrs9832727
openSNPrs9832727
23andMers9832727
SNPshotrs9832727
SNPdbers9832727
MSV3drs9832727
GWAS Ctlgrs9832727
GMAF0.3338
Max Magnitude0
? (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 6E-29
Odds Ratio 0 None