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rs789560

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs789560(A;A)
Make rs789560(A;C)
ReferenceGRCh38 38.1/142
Chromosome12
Position69938047
GeneMYRFL
is asnp
is mentioned by
dbSNPrs789560
dbSNP (classic)rs789560
ClinGenrs789560
ebirs789560
HLIrs789560
Exacrs789560
Gnomadrs789560
Varsomers789560
LitVarrs789560
Maprs789560
PheGenIrs789560
Biobankrs789560
1000 genomesrs789560
hgdprs789560
ensemblrs789560
geneviewrs789560
scholarrs789560
googlers789560
pharmgkbrs789560
gwascentralrs789560
openSNPrs789560
23andMers789560
SNPshotrs789560
SNPdbers789560
MSV3drs789560
GWAS Ctlgrs789560
GMAF0.08586
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 18951430]
Trait Attention-deficit/hyperactivity disorder and conduct disorder
Title Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study
Risk Allele G
P-val 0.000007
Odds Ratio NR NR