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rs7992643

From SNPedia

Orientationplus
Stabilizedplus
Make rs7992643(C;C)
Make rs7992643(C;G)
Make rs7992643(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position99902784
GeneCLYBL, LOC101927437
is asnp
is mentioned by
dbSNPrs7992643
ebirs7992643
HLIrs7992643
Exacrs7992643
Varsomers7992643
Maprs7992643
PheGenIrs7992643
hapmaprs7992643
1000 genomesrs7992643
hgdprs7992643
ensemblrs7992643
gopubmedrs7992643
geneviewrs7992643
scholarrs7992643
googlers7992643
pharmgkbrs7992643
gwascentralrs7992643
openSNPrs7992643
23andMers7992643
23andMe allrs7992643
SNP Nexus

SNPshotrs7992643
SNPdbers7992643
MSV3drs7992643
GWAS Ctlgrs7992643
GMAF0.4986
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 18821565]
Trait Attention deficit hyperactivity disorder
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 0.000005
Odds Ratio NR NR


GET Evidence
rs7992643
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.540323
summary