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rs2823819

From SNPedia

Orientationplus
Stabilizedplus
Make rs2823819(A;A)
Make rs2823819(A;G)
Make rs2823819(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position16455971
GeneLINC00478
is asnp
is mentioned by
dbSNPrs2823819
ebirs2823819
HLIrs2823819
Exacrs2823819
Varsomers2823819
Maprs2823819
PheGenIrs2823819
hapmaprs2823819
1000 genomesrs2823819
hgdprs2823819
ensemblrs2823819
gopubmedrs2823819
geneviewrs2823819
scholarrs2823819
googlers2823819
pharmgkbrs2823819
gwascentralrs2823819
openSNPrs2823819
23andMers2823819
23andMe allrs2823819
SNP Nexus

SNPshotrs2823819
SNPdbers2823819
MSV3drs2823819
GWAS Ctlgrs2823819
GMAF0.1703
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20732626OA-icon.png]
Trait
Title Family-Based Genome-Wide Association Scan of Attention-Deficit/Hyperactivity Disorder
Risk Allele C
P-val 7E-7
Odds Ratio 1.65 [NR]


[PMID 20017974OA-icon.png] Simultaneous analysis of all single-nucleotide polymorphisms in genome-wide association study of rheumatoid arthritis.