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rs1471225

From SNPedia

Orientationplus
Stabilizedplus
Make rs1471225(C;C)
Make rs1471225(C;T)
Make rs1471225(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position29596192
is asnp
is mentioned by
dbSNPrs1471225
ebirs1471225
HLIrs1471225
Exacrs1471225
Varsomers1471225
Maprs1471225
PheGenIrs1471225
hapmaprs1471225
1000 genomesrs1471225
hgdprs1471225
ensemblrs1471225
gopubmedrs1471225
geneviewrs1471225
scholarrs1471225
googlers1471225
pharmgkbrs1471225
gwascentralrs1471225
openSNPrs1471225
23andMers1471225
23andMe allrs1471225
SNP Nexus

SNPshotrs1471225
SNPdbers1471225
MSV3drs1471225
GWAS Ctlgrs1471225
GMAF0.4201
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 0.000008
Odds Ratio NR NR


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


GET Evidence
rs1471225
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.4375
summary