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rs7495052

From SNPedia

Orientationplus
Stabilizedplus
Make rs7495052(C;C)
Make rs7495052(C;T)
Make rs7495052(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position92008799
GeneSLCO3A1
is asnp
is mentioned by
dbSNPrs7495052
ebirs7495052
HLIrs7495052
Exacrs7495052
Varsomers7495052
Maprs7495052
PheGenIrs7495052
hapmaprs7495052
1000 genomesrs7495052
hgdprs7495052
ensemblrs7495052
gopubmedrs7495052
geneviewrs7495052
scholarrs7495052
googlers7495052
pharmgkbrs7495052
gwascentralrs7495052
openSNPrs7495052
23andMers7495052
23andMe allrs7495052
SNP Nexus

SNPshotrs7495052
SNPdbers7495052
MSV3drs7495052
GWAS Ctlgrs7495052
GMAF0.477
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18821565]
Trait Inattentive symptoms
Title Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations
Risk Allele
P-val 0.000003
Odds Ratio NR NR


[PMID 20148275OA-icon.png] Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.


GET Evidence
rs7495052
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.4375
summary