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rs1078373

From SNPedia

Orientationplus
Stabilizedplus
Make rs1078373(A;A)
Make rs1078373(A;G)
Make rs1078373(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position31310224
GeneTSHZ3
is asnp
is mentioned by
dbSNPrs1078373
ebirs1078373
HLIrs1078373
Exacrs1078373
Varsomers1078373
Maprs1078373
PheGenIrs1078373
hapmaprs1078373
1000 genomesrs1078373
hgdprs1078373
ensemblrs1078373
gopubmedrs1078373
geneviewrs1078373
scholarrs1078373
googlers1078373
pharmgkbrs1078373
gwascentralrs1078373
openSNPrs1078373
23andMers1078373
23andMe allrs1078373
SNP Nexus

SNPshotrs1078373
SNPdbers1078373
MSV3drs1078373
GWAS Ctlgrs1078373
GMAF0.3026
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 0.000006
Odds Ratio NR NR

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


GET Evidence
rs1078373
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.289062
summary