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rs1897031

From SNPedia

Orientationminus
Stabilizedminus
Make rs1897031(C;C)
Make rs1897031(C;T)
Make rs1897031(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position54049268
GeneUNC13C
is asnp
is mentioned by
dbSNPrs1897031
ebirs1897031
HLIrs1897031
Exacrs1897031
Varsomers1897031
Maprs1897031
PheGenIrs1897031
hapmaprs1897031
1000 genomesrs1897031
hgdprs1897031
ensemblrs1897031
gopubmedrs1897031
geneviewrs1897031
scholarrs1897031
googlers1897031
pharmgkbrs1897031
gwascentralrs1897031
openSNPrs1897031
23andMers1897031
23andMe allrs1897031
SNP Nexus

SNPshotrs1897031
SNPdbers1897031
MSV3drs1897031
GWAS Ctlgrs1897031
GMAF0.2025
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 0.000001
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 1 x 10^-6) for pattern recognition memory (PRM) percent correct in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs1897031
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.944444
summary