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rs10983238

From SNPedia

Orientationplus
Stabilizedplus
Make rs10983238(C;C)
Make rs10983238(C;G)
Make rs10983238(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position116571404
GeneASTN2
is asnp
is mentioned by
dbSNPrs10983238
ebirs10983238
HLIrs10983238
Exacrs10983238
Varsomers10983238
Maprs10983238
PheGenIrs10983238
hapmaprs10983238
1000 genomesrs10983238
hgdprs10983238
ensemblrs10983238
gopubmedrs10983238
geneviewrs10983238
scholarrs10983238
googlers10983238
pharmgkbrs10983238
gwascentralrs10983238
openSNPrs10983238
23andMers10983238
23andMe allrs10983238
SNP Nexus

SNPshotrs10983238
SNPdbers10983238
MSV3drs10983238
GWAS Ctlgrs10983238
GMAF0.1455
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 18839057]
Trait Attention-deficit/hyperactivity disorder
Title Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
Risk Allele
P-val 1E-7
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
rs10983238
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.171875
summary