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rs10895959

From SNPedia

Orientationplus
Stabilizedplus
Make rs10895959(A;A)
Make rs10895959(A;G)
Make rs10895959(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position106459435
is asnp
is mentioned by
dbSNPrs10895959
ebirs10895959
HLIrs10895959
Exacrs10895959
Varsomers10895959
Maprs10895959
PheGenIrs10895959
hapmaprs10895959
1000 genomesrs10895959
hgdprs10895959
ensemblrs10895959
gopubmedrs10895959
geneviewrs10895959
scholarrs10895959
googlers10895959
pharmgkbrs10895959
gwascentralrs10895959
openSNPrs10895959
23andMers10895959
23andMe allrs10895959
SNP Nexus

SNPshotrs10895959
SNPdbers10895959
MSV3drs10895959
GWAS Ctlgrs10895959
GMAF0.3737
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000003
Odds Ratio NR NR


GET Evidence
rs10895959
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.703125
summary