Have questions? Visit https://www.reddit.com/r/SNPedia

rs10227331

From SNPedia

Orientationplus
Stabilizedplus
Make rs10227331(A;A)
Make rs10227331(A;T)
Make rs10227331(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position157502244
GeneTGFB3
is asnp
is mentioned by
dbSNPrs10227331
ebirs10227331
HLIrs10227331
Exacrs10227331
Varsomers10227331
Maprs10227331
PheGenIrs10227331
hapmaprs10227331
1000 genomesrs10227331
hgdprs10227331
ensemblrs10227331
gopubmedrs10227331
geneviewrs10227331
scholarrs10227331
googlers10227331
pharmgkbrs10227331
gwascentralrs10227331
openSNPrs10227331
23andMers10227331
23andMe allrs10227331
SNP Nexus

SNPshotrs10227331
SNPdbers10227331
MSV3drs10227331
GWAS Ctlgrs10227331
GMAF0.4357
Max Magnitude
? (A;A) (A;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 0.000004
Odds Ratio NR NR


GET Evidence
rs10227331
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.390625
summary