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rs130575

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs130575(A;G)
Make rs130575(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position34463801
is asnp
is mentioned by
dbSNPrs130575
ebirs130575
HLIrs130575
Exacrs130575
Varsomers130575
Maprs130575
PheGenIrs130575
hapmaprs130575
1000 genomesrs130575
hgdprs130575
ensemblrs130575
gopubmedrs130575
geneviewrs130575
scholarrs130575
googlers130575
pharmgkbrs130575
gwascentralrs130575
openSNPrs130575
23andMers130575
23andMe allrs130575
SNP Nexus

SNPshotrs130575
SNPdbers130575
MSV3drs130575
GWAS Ctlgrs130575
GMAF0.1359
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18821565]
Trait Attention deficit hyperactivity disorder
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 18937294OA-icon.png] Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.


GET Evidence
rs130575
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary