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rs7612209

From SNPedia

Orientationplus
Stabilizedplus
Make rs7612209(A;A)
Make rs7612209(A;G)
Make rs7612209(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position177879201
GeneLOC102724550, RP11-91K9.1
is asnp
is mentioned by
dbSNPrs7612209
ebirs7612209
HLIrs7612209
Exacrs7612209
Varsomers7612209
Maprs7612209
PheGenIrs7612209
hapmaprs7612209
1000 genomesrs7612209
hgdprs7612209
ensemblrs7612209
gopubmedrs7612209
geneviewrs7612209
scholarrs7612209
googlers7612209
pharmgkbrs7612209
gwascentralrs7612209
openSNPrs7612209
23andMers7612209
23andMe allrs7612209
SNP Nexus

SNPshotrs7612209
SNPdbers7612209
MSV3drs7612209
GWAS Ctlgrs7612209
GMAF0.4725
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 0.000004
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 4 x 10^-6) for intra-extra dimensional set shift (IED) EDS errors in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs7612209
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.476562
summary