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rs874426

From SNPedia

Orientationminus
Stabilizedminus
Make rs874426(G;G)
Make rs874426(G;T)
Make rs874426(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position19548016
GeneNAV2
is asnp
is mentioned by
dbSNPrs874426
ebirs874426
HLIrs874426
Exacrs874426
Varsomers874426
Maprs874426
PheGenIrs874426
hapmaprs874426
1000 genomesrs874426
hgdprs874426
ensemblrs874426
gopubmedrs874426
geneviewrs874426
scholarrs874426
googlers874426
pharmgkbrs874426
gwascentralrs874426
openSNPrs874426
23andMers874426
23andMe allrs874426
SNP Nexus

SNPshotrs874426
SNPdbers874426
MSV3drs874426
GWAS Ctlgrs874426
GMAF0.3912
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 18937294OA-icon.png]
Trait Attention deficit hyperactivity disorder (time to onset)
Title Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder
Risk Allele C
P-val 0.000004
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
rs874426
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.59375
summary