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rs1155865

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1155865(A;G)
Make rs1155865(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position66868139
is asnp
is mentioned by
dbSNPrs1155865
ebirs1155865
HLIrs1155865
Exacrs1155865
Varsomers1155865
Maprs1155865
PheGenIrs1155865
hapmaprs1155865
1000 genomesrs1155865
hgdprs1155865
ensemblrs1155865
gopubmedrs1155865
geneviewrs1155865
scholarrs1155865
googlers1155865
pharmgkbrs1155865
gwascentralrs1155865
openSNPrs1155865
23andMers1155865
23andMe allrs1155865
SNP Nexus

SNPshotrs1155865
SNPdbers1155865
MSV3drs1155865
GWAS Ctlgrs1155865
GMAF0.2094
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs1155865
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, Boston Naming Test



GET Evidence
rs1155865
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.757812
summary