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rs4713586

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs4713586(C;C)
Make rs4713586(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32691805
is asnp
is mentioned by
dbSNPrs4713586
ebirs4713586
HLIrs4713586
Exacrs4713586
Varsomers4713586
Maprs4713586
PheGenIrs4713586
hapmaprs4713586
1000 genomesrs4713586
hgdprs4713586
ensemblrs4713586
gopubmedrs4713586
geneviewrs4713586
scholarrs4713586
googlers4713586
pharmgkbrs4713586
gwascentralrs4713586
openSNPrs4713586
23andMers4713586
23andMe allrs4713586
SNP Nexus

SNPshotrs4713586
SNPdbers4713586
MSV3drs4713586
GWAS Ctlgrs4713586
GMAF0.07989
Max Magnitude0
? (C;C) (C;T) (T;T) 28
rs4713586 is one of three HLA region SNPs used to tag the DQ2.2 haplotype in gs221. [PMID 18509540OA-icon.png]