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rs1861050

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1861050(C;T)
Make rs1861050(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position15480736
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs1861050
ebirs1861050
HLIrs1861050
Exacrs1861050
Varsomers1861050
Maprs1861050
PheGenIrs1861050
hapmaprs1861050
1000 genomesrs1861050
hgdprs1861050
ensemblrs1861050
gopubmedrs1861050
geneviewrs1861050
scholarrs1861050
googlers1861050
pharmgkbrs1861050
gwascentralrs1861050
openSNPrs1861050
23andMers1861050
23andMe allrs1861050
SNP Nexus

SNPshotrs1861050
SNPdbers1861050
MSV3drs1861050
GWAS Ctlgrs1861050
GMAF0.1107
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20585324OA-icon.png]
Trait Conduct disorder (case status)
Title Genome-wide association study of conduct disorder symptomatology
Risk Allele
P-val 0.000008
Odds Ratio 1.63 [1.31-2.01]


ClinVar
Risk rs1861050(T;T)
Alt rs1861050(T;T)
Reference rs1861050(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene CC2D2A
CLNDBN not specified
Reversed 0
HGVS NC_000004.11:g.15482360C>T
CLNSRC ClinVar University of Chicago
CLNACC RCV000114165.2,