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rs1071817

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1071817(A;A)
Make rs1071817(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356751
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1071817
ebirs1071817
HLIrs1071817
Exacrs1071817
Varsomers1071817
Maprs1071817
PheGenIrs1071817
hapmaprs1071817
1000 genomesrs1071817
hgdprs1071817
ensemblrs1071817
gopubmedrs1071817
geneviewrs1071817
scholarrs1071817
googlers1071817
pharmgkbrs1071817
gwascentralrs1071817
openSNPrs1071817
23andMers1071817
23andMe allrs1071817
SNP Nexus

SNPshotrs1071817
SNPdbers1071817
MSV3drs1071817
GWAS Ctlgrs1071817
GMAF0.3246
Max Magnitude0
ClinVar
Risk rs1071817(A,G,T;A,G,T)
Alt rs1071817(A,G,T;A,G,T)
Reference rs1071817(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324528G>A; NC_000006.11:g.31324528G>C; NC_000006.11:g.31324528G>T
CLNSRC
CLNACC