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rs7577925

From SNPedia

Orientationplus
Stabilizedplus
Make rs7577925(A;A)
Make rs7577925(A;G)
Make rs7577925(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position133282947
GeneAC010890.1, NCKAP5
is asnp
is mentioned by
dbSNPrs7577925
ebirs7577925
HLIrs7577925
Exacrs7577925
Varsomers7577925
Maprs7577925
PheGenIrs7577925
hapmaprs7577925
1000 genomesrs7577925
hgdprs7577925
ensemblrs7577925
gopubmedrs7577925
geneviewrs7577925
scholarrs7577925
googlers7577925
pharmgkbrs7577925
gwascentralrs7577925
openSNPrs7577925
23andMers7577925
23andMe allrs7577925
SNP Nexus

SNPshotrs7577925
SNPdbers7577925
MSV3drs7577925
GWAS Ctlgrs7577925
GMAF0.354
Max Magnitude
? (A;A) (A;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 0.000003
Odds Ratio NR NR


GET Evidence
rs7577925
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.320312
summary