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rs7172689

From SNPedia

Orientationplus
Stabilizedplus
Make rs7172689(C;C)
Make rs7172689(C;T)
Make rs7172689(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position81241354
GeneIL16
is asnp
is mentioned by
dbSNPrs7172689
ebirs7172689
HLIrs7172689
Exacrs7172689
Varsomers7172689
Maprs7172689
PheGenIrs7172689
hapmaprs7172689
1000 genomesrs7172689
hgdprs7172689
ensemblrs7172689
gopubmedrs7172689
geneviewrs7172689
scholarrs7172689
googlers7172689
pharmgkbrs7172689
gwascentralrs7172689
openSNPrs7172689
23andMers7172689
23andMe allrs7172689
SNP Nexus

SNPshotrs7172689
SNPdbers7172689
MSV3drs7172689
GWAS Ctlgrs7172689
GMAF0.1979
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000004
Odds Ratio NR NR


GET Evidence
rs7172689
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.163934
summary