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rs12721836

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs12721836(C;C)
Make rs12721836(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356399
GeneHLA-B
is asnp
is mentioned by
dbSNPrs12721836
ebirs12721836
HLIrs12721836
Exacrs12721836
Varsomers12721836
Maprs12721836
PheGenIrs12721836
hapmaprs12721836
1000 genomesrs12721836
hgdprs12721836
ensemblrs12721836
gopubmedrs12721836
geneviewrs12721836
scholarrs12721836
googlers12721836
pharmgkbrs12721836
gwascentralrs12721836
openSNPrs12721836
23andMers12721836
23andMe allrs12721836
SNP Nexus

SNPshotrs12721836
SNPdbers12721836
MSV3drs12721836
GWAS Ctlgrs12721836
GMAF0.1589
Max Magnitude0
ClinVar
Risk rs12721836(C;C)
Alt rs12721836(C;C)
Reference rs12721836(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324176C>G
CLNSRC
CLNACC