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rs7816032

From SNPedia

Orientationplus
Stabilizedplus
Make rs7816032(C;C)
Make rs7816032(C;T)
Make rs7816032(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position19929380
is asnp
is mentioned by
dbSNPrs7816032
ebirs7816032
HLIrs7816032
Exacrs7816032
Varsomers7816032
Maprs7816032
PheGenIrs7816032
hapmaprs7816032
1000 genomesrs7816032
hgdprs7816032
ensemblrs7816032
gopubmedrs7816032
geneviewrs7816032
scholarrs7816032
googlers7816032
pharmgkbrs7816032
gwascentralrs7816032
openSNPrs7816032
23andMers7816032
23andMe allrs7816032
SNP Nexus

SNPshotrs7816032
SNPdbers7816032
MSV3drs7816032
GWAS Ctlgrs7816032
GMAF0.3062
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 0.000002
Odds Ratio NR NR


GET Evidence
rs7816032
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.375
summary