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rs12721849

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs12721849(C;G)
Make rs12721849(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356333
GeneHLA-B
is asnp
is mentioned by
dbSNPrs12721849
ebirs12721849
HLIrs12721849
Exacrs12721849
Varsomers12721849
Maprs12721849
PheGenIrs12721849
hapmaprs12721849
1000 genomesrs12721849
hgdprs12721849
ensemblrs12721849
gopubmedrs12721849
geneviewrs12721849
scholarrs12721849
googlers12721849
pharmgkbrs12721849
gwascentralrs12721849
openSNPrs12721849
23andMers12721849
23andMe allrs12721849
SNP Nexus

SNPshotrs12721849
SNPdbers12721849
MSV3drs12721849
GWAS Ctlgrs12721849
GMAF0.04637
Max Magnitude0
ClinVar
Risk rs12721849(A,G,T;A,G,T)
Alt rs12721849(A,G,T;A,G,T)
Reference rs12721849(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324110G>A; NC_000006.11:g.31324110G>C; NC_000006.11:g.31324110G>T
CLNSRC
CLNACC