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rs12721829

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs12721829(A;A)
Make rs12721829(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356431
GeneHLA-B
is asnp
is mentioned by
dbSNPrs12721829
ebirs12721829
HLIrs12721829
Exacrs12721829
Varsomers12721829
Maprs12721829
PheGenIrs12721829
hapmaprs12721829
1000 genomesrs12721829
hgdprs12721829
ensemblrs12721829
gopubmedrs12721829
geneviewrs12721829
scholarrs12721829
googlers12721829
pharmgkbrs12721829
gwascentralrs12721829
openSNPrs12721829
23andMers12721829
23andMe allrs12721829
SNP Nexus

SNPshotrs12721829
SNPdbers12721829
MSV3drs12721829
GWAS Ctlgrs12721829
GMAF0.2534
Max Magnitude0
ClinVar
Risk rs12721829(A,G,T;A,G,T)
Alt rs12721829(A,G,T;A,G,T)
Reference rs12721829(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324208G>A; NC_000006.11:g.31324208G>C; NC_000006.11:g.31324208G>T
CLNSRC
CLNACC