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

rs17079773

From SNPedia

Orientationplus
Stabilizedplus
Make rs17079773(C;C)
Make rs17079773(C;T)
Make rs17079773(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position24024245
GeneSPATA13
is asnp
is mentioned by
dbSNPrs17079773
ebirs17079773
HLIrs17079773
Exacrs17079773
Varsomers17079773
Maprs17079773
PheGenIrs17079773
hapmaprs17079773
1000 genomesrs17079773
hgdprs17079773
ensemblrs17079773
gopubmedrs17079773
geneviewrs17079773
scholarrs17079773
googlers17079773
pharmgkbrs17079773
gwascentralrs17079773
openSNPrs17079773
23andMers17079773
23andMe allrs17079773
SNP Nexus

SNPshotrs17079773
SNPdbers17079773
MSV3drs17079773
GWAS Ctlgrs17079773
GMAF0.1915
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 0.000005
Odds Ratio NR NR


[PMID 20145962OA-icon.png] Molecular genetics of attention-deficit/hyperactivity disorder: an overview.


GET Evidence
rs17079773
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary