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rs111301312

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111301312(G;G)
Make rs111301312(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354331
GeneHLA-B
is asnp
is mentioned by
dbSNPrs111301312
ebirs111301312
HLIrs111301312
Exacrs111301312
Varsomers111301312
Maprs111301312
PheGenIrs111301312
hapmaprs111301312
1000 genomesrs111301312
hgdprs111301312
ensemblrs111301312
gopubmedrs111301312
geneviewrs111301312
scholarrs111301312
googlers111301312
pharmgkbrs111301312
gwascentralrs111301312
openSNPrs111301312
23andMers111301312
23andMe allrs111301312
SNP Nexus

SNPshotrs111301312
SNPdbers111301312
MSV3drs111301312
GWAS Ctlgrs111301312
GMAF0.04224
Max Magnitude0
ClinVar
Risk rs111301312(G,C;G,C)
Alt rs111301312(G,C;G,C)
Reference rs111301312(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322108T>G
CLNSRC
CLNACC