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rs10797919

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;G) 0 common in complete genomics
Make rs10797919(C;C)
Make rs10797919(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position183883780
GeneRGL1
is asnp
is mentioned by
dbSNPrs10797919
ebirs10797919
HLIrs10797919
Exacrs10797919
Varsomers10797919
Maprs10797919
PheGenIrs10797919
hapmaprs10797919
1000 genomesrs10797919
hgdprs10797919
ensemblrs10797919
gopubmedrs10797919
geneviewrs10797919
scholarrs10797919
googlers10797919
pharmgkbrs10797919
gwascentralrs10797919
openSNPrs10797919
23andMers10797919
23andMe allrs10797919
SNP Nexus

SNPshotrs10797919
SNPdbers10797919
MSV3drs10797919
GWAS Ctlgrs10797919
GMAF0.4454
Max Magnitude0
? (C;C) (C;G) (G;G) 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 0.000009
Odds Ratio NR NR



GET Evidence
rs10797919
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.439394
summary