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rs41441749

From SNPedia

Orientationplus
Stabilizedplus
Make rs41441749(C;C)
Make rs41441749(C;T)
Make rs41441749(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position18791492
is asnp
is mentioned by
dbSNPrs41441749
ebirs41441749
HLIrs41441749
Exacrs41441749
Varsomers41441749
Maprs41441749
PheGenIrs41441749
hapmaprs41441749
1000 genomesrs41441749
hgdprs41441749
ensemblrs41441749
gopubmedrs41441749
geneviewrs41441749
scholarrs41441749
googlers41441749
pharmgkbrs41441749
gwascentralrs41441749
openSNPrs41441749
23andMers41441749
23andMe allrs41441749
SNP Nexus

SNPshotrs41441749
SNPdbers41441749
MSV3drs41441749
GWAS Ctlgrs41441749
GMAF0.1722
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18821565]
Trait Hyperactive-impulsive 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 0.000001
Odds Ratio NR NR


GET Evidence
rs41441749
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.226562
summary