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rs11139399

From SNPedia

Orientationplus
Stabilizedplus
Make rs11139399(C;C)
Make rs11139399(C;T)
Make rs11139399(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position81757826
GeneRP11-154D17.1
is asnp
is mentioned by
dbSNPrs11139399
ebirs11139399
HLIrs11139399
Exacrs11139399
Varsomers11139399
Maprs11139399
PheGenIrs11139399
hapmaprs11139399
1000 genomesrs11139399
hgdprs11139399
ensemblrs11139399
gopubmedrs11139399
geneviewrs11139399
scholarrs11139399
googlers11139399
pharmgkbrs11139399
gwascentralrs11139399
openSNPrs11139399
23andMers11139399
23andMe allrs11139399
SNP Nexus

SNPshotrs11139399
SNPdbers11139399
MSV3drs11139399
GWAS Ctlgrs11139399
GMAF0.489
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22745009OA-icon.png]
Trait
Title Multiple loci influencing hippocampal degeneration identified by genome scan.
Risk Allele C
P-val 0.000001
Odds Ratio None None