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rs1442190

From SNPedia

Orientationplus
Stabilizedplus
Make rs1442190(A;A)
Make rs1442190(A;G)
Make rs1442190(G;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position40971838
GeneCNTN1
is asnp
is mentioned by
dbSNPrs1442190
ebirs1442190
HLIrs1442190
Exacrs1442190
Varsomers1442190
Maprs1442190
PheGenIrs1442190
hapmaprs1442190
1000 genomesrs1442190
hgdprs1442190
ensemblrs1442190
gopubmedrs1442190
geneviewrs1442190
scholarrs1442190
googlers1442190
pharmgkbrs1442190
gwascentralrs1442190
openSNPrs1442190
23andMers1442190
23andMe allrs1442190
SNP Nexus

SNPshotrs1442190
SNPdbers1442190
MSV3drs1442190
GWAS Ctlgrs1442190
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24842889OA-icon.png]
Trait Parkinson's disease
Title Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
Risk Allele
P-val 2E-27
Odds Ratio 3.72 [2.98-4.64]