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rs272000

From SNPedia

Orientationminus
Stabilizedminus
Make rs272000(C;C)
Make rs272000(C;G)
Make rs272000(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position115898219
is asnp
is mentioned by
dbSNPrs272000
ebirs272000
HLIrs272000
Exacrs272000
Varsomers272000
Maprs272000
PheGenIrs272000
hapmaprs272000
1000 genomesrs272000
hgdprs272000
ensemblrs272000
gopubmedrs272000
geneviewrs272000
scholarrs272000
googlers272000
pharmgkbrs272000
gwascentralrs272000
openSNPrs272000
23andMers272000
23andMe allrs272000
SNP Nexus

SNPshotrs272000
SNPdbers272000
MSV3drs272000
GWAS Ctlgrs272000
GMAF0.4366
Max Magnitude
? (C;C) (C;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 0.000009
Odds Ratio NR NR

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

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


GET Evidence
rs272000
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.515625
summary