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Rs2352904

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Orientationplus
Make rs2352904(A;A)
Make rs2352904(A;C)
Make rs2352904(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position48903598
is asnp
is mentioned by
dbSNPrs2352904
PheGenIrs2352904
nextbiors2352904
hapmaprs2352904
1000 genomesrs2352904
hgdprs2352904
ensemblrs2352904
gopubmedrs2352904
geneviewrs2352904
scholarrs2352904
googlers2352904
pharmgkbrs2352904
gwascentralrs2352904
openSNPrs2352904
23andMers2352904
23andMe allrs2352904
SNP Nexus

SNPshotrs2352904
SNPdbers2352904
MSV3drs2352904
GMAF0.4936
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs2352904
PubMedID [PMID 17903297OA-icon.png]
Condition Cognitive test performance
Gene Intergenic
Risk Allele
pValue 2.00E-006
OR NA
95% CI


[PMID 17903297OA-icon.png] non sig. gwas, top 25 GEE p-values, visual memory and organization



GET Evidence
rs2352904
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.578125
summary