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rs16966122

From SNPedia

Orientationplus
Stabilizedplus
Make rs16966122(A;A)
Make rs16966122(A;G)
Make rs16966122(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position31667558
is asnp
is mentioned by
dbSNPrs16966122
ebirs16966122
HLIrs16966122
Exacrs16966122
Varsomers16966122
Maprs16966122
PheGenIrs16966122
hapmaprs16966122
1000 genomesrs16966122
hgdprs16966122
ensemblrs16966122
gopubmedrs16966122
geneviewrs16966122
scholarrs16966122
googlers16966122
pharmgkbrs16966122
gwascentralrs16966122
openSNPrs16966122
23andMers16966122
23andMe allrs16966122
SNP Nexus

SNPshotrs16966122
SNPdbers16966122
MSV3drs16966122
GWAS Ctlgrs16966122
GMAF0.1198
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23496005]
Trait Narcolepsy with cataplexy
Title Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.
Risk Allele
P-val 2E-6
Odds Ratio 1.60 [NR] unit decrease