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rs9315702

From SNPedia

Orientationplus
Stabilizedplus
Make rs9315702(A;A)
Make rs9315702(A;C)
Make rs9315702(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position39543931
GeneLHFP
is asnp
is mentioned by
dbSNPrs9315702
ebirs9315702
HLIrs9315702
Exacrs9315702
Varsomers9315702
Maprs9315702
PheGenIrs9315702
hapmaprs9315702
1000 genomesrs9315702
hgdprs9315702
ensemblrs9315702
gopubmedrs9315702
geneviewrs9315702
scholarrs9315702
googlers9315702
pharmgkbrs9315702
gwascentralrs9315702
openSNPrs9315702
23andMers9315702
23andMe allrs9315702
SNP Nexus

SNPshotrs9315702
SNPdbers9315702
MSV3drs9315702
GWAS Ctlgrs9315702
GMAF0.286
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22745009OA-icon.png]
Trait
Title Multiple loci influencing hippocampal degeneration identified by genome scan.
Risk Allele A
P-val 2E-8
Odds Ratio None None