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rs7665090

From SNPedia

Orientationplus
Stabilizedplus
Make rs7665090(A;A)
Make rs7665090(A;G)
Make rs7665090(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position102630446
GeneMANBA
is asnp
is mentioned by
dbSNPrs7665090
ebirs7665090
HLIrs7665090
Exacrs7665090
Varsomers7665090
Maprs7665090
PheGenIrs7665090
hapmaprs7665090
1000 genomesrs7665090
hgdprs7665090
ensemblrs7665090
gopubmedrs7665090
geneviewrs7665090
scholarrs7665090
googlers7665090
pharmgkbrs7665090
gwascentralrs7665090
openSNPrs7665090
23andMers7665090
23andMe allrs7665090
SNP Nexus

SNPshotrs7665090
SNPdbers7665090
MSV3drs7665090
GWAS Ctlgrs7665090
GMAF0.4504
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21399635OA-icon.png]
Trait
Title Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis
Risk Allele C
P-val 4E-12
Odds Ratio 1.2600 [1.18-1.34]


[PMID 23543094OA-icon.png] Testing for associations between loci and environmental gradients using latent factor mixed models.