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rs7892812

From SNPedia

Orientationplus
Stabilizedplus
Make rs7892812(A;A)
Make rs7892812(A;G)
Make rs7892812(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position8426212
is asnp
is mentioned by
dbSNPrs7892812
ebirs7892812
HLIrs7892812
Exacrs7892812
Varsomers7892812
Maprs7892812
PheGenIrs7892812
hapmaprs7892812
1000 genomesrs7892812
hgdprs7892812
ensemblrs7892812
gopubmedrs7892812
geneviewrs7892812
scholarrs7892812
googlers7892812
pharmgkbrs7892812
gwascentralrs7892812
openSNPrs7892812
23andMers7892812
23andMe allrs7892812
SNP Nexus

SNPshotrs7892812
SNPdbers7892812
MSV3drs7892812
GWAS Ctlgrs7892812
GMAF0.3851
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19734545OA-icon.png]
Trait Cognitive performance
Title A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery
Risk Allele
P-val 0.000008
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 8 x 10^-6) for spatial span (SSP) length in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs7892812
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.586957
summary