Have questions? Visit https://www.reddit.com/r/SNPedia

rs2241685

From SNPedia

Orientationplus
Stabilizedplus
Make rs2241685(C;C)
Make rs2241685(C;T)
Make rs2241685(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position1922221
GeneMYT1L
is asnp
is mentioned by
dbSNPrs2241685
ebirs2241685
HLIrs2241685
Exacrs2241685
Varsomers2241685
Maprs2241685
PheGenIrs2241685
hapmaprs2241685
1000 genomesrs2241685
hgdprs2241685
ensemblrs2241685
gopubmedrs2241685
geneviewrs2241685
scholarrs2241685
googlers2241685
pharmgkbrs2241685
gwascentralrs2241685
openSNPrs2241685
23andMers2241685
23andMe allrs2241685
SNP Nexus

SNPshotrs2241685
SNPdbers2241685
MSV3drs2241685
GWAS Ctlgrs2241685
GMAF0.1878
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000008
Odds Ratio NR NR


GET Evidence
rs2241685
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary