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rs1071652

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1071652(G;T)
Make rs1071652(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356424
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1071652
ebirs1071652
HLIrs1071652
Exacrs1071652
Varsomers1071652
Maprs1071652
PheGenIrs1071652
hapmaprs1071652
1000 genomesrs1071652
hgdprs1071652
ensemblrs1071652
gopubmedrs1071652
geneviewrs1071652
scholarrs1071652
googlers1071652
pharmgkbrs1071652
gwascentralrs1071652
openSNPrs1071652
23andMers1071652
23andMe allrs1071652
SNP Nexus

SNPshotrs1071652
SNPdbers1071652
MSV3drs1071652
GWAS Ctlgrs1071652
Max Magnitude0
ClinVar
Risk rs1071652(A,C,T;A,C,T)
Alt rs1071652(A,C,T;A,C,T)
Reference rs1071652(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324201C>A; NC_000006.11:g.31324201C>G; NC_000006.11:g.31324201C>T
CLNSRC
CLNACC