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rs10279573

From SNPedia

Orientationplus
Stabilizedplus
Make rs10279573(C;C)
Make rs10279573(C;T)
Make rs10279573(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position110827165
GeneIMMP2L
is asnp
is mentioned by
dbSNPrs10279573
ebirs10279573
HLIrs10279573
Exacrs10279573
Varsomers10279573
Maprs10279573
PheGenIrs10279573
hapmaprs10279573
1000 genomesrs10279573
hgdprs10279573
ensemblrs10279573
gopubmedrs10279573
geneviewrs10279573
scholarrs10279573
googlers10279573
pharmgkbrs10279573
gwascentralrs10279573
openSNPrs10279573
23andMers10279573
23andMe allrs10279573
SNP Nexus

SNPshotrs10279573
SNPdbers10279573
MSV3drs10279573
GWAS Ctlgrs10279573
GMAF0.1878
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000003
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 3 x 10^-6) for intra-extra dimensional set shift (IED) EDS errors in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs10279573
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.1875
summary