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rs17086609

From SNPedia

Orientationplus
Stabilizedplus
Make rs17086609(A;A)
Make rs17086609(A;G)
Make rs17086609(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position28355574
GeneFLT1
is asnp
is mentioned by
dbSNPrs17086609
ebirs17086609
HLIrs17086609
Exacrs17086609
Varsomers17086609
Maprs17086609
PheGenIrs17086609
hapmaprs17086609
1000 genomesrs17086609
hgdprs17086609
ensemblrs17086609
gopubmedrs17086609
geneviewrs17086609
scholarrs17086609
googlers17086609
pharmgkbrs17086609
gwascentralrs17086609
openSNPrs17086609
23andMers17086609
23andMe allrs17086609
SNP Nexus

SNPshotrs17086609
SNPdbers17086609
MSV3drs17086609
GWAS Ctlgrs17086609
GMAF0.2998
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 0.000005
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 5 x 10^-6) for intra-extra dimensional set shift (IED) EDS errors in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs17086609
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.242188
summary