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rs7616215

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 Normal
Make rs7616215(C;C)
Make rs7616215(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position46164194
is asnp
is mentioned by
dbSNPrs7616215
ebirs7616215
HLIrs7616215
Exacrs7616215
Varsomers7616215
Maprs7616215
PheGenIrs7616215
hapmaprs7616215
1000 genomesrs7616215
hgdprs7616215
ensemblrs7616215
gopubmedrs7616215
geneviewrs7616215
scholarrs7616215
googlers7616215
pharmgkbrs7616215
gwascentralrs7616215
openSNPrs7616215
23andMers7616215
23andMe allrs7616215
SNP Nexus

SNPshotrs7616215
SNPdbers7616215
MSV3drs7616215
GWAS Ctlgrs7616215
GMAF0.3242
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23291587OA-icon.png]
Trait Behcet's disease
Title Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.
Risk Allele C
P-val 4E-13
Odds Ratio 1.39 [1.27-1.52]