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rs7750864

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs7750864(C;C)
Make rs7750864(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355253
GeneHLA-B
is asnp
is mentioned by
dbSNPrs7750864
ebirs7750864
HLIrs7750864
Exacrs7750864
Varsomers7750864
Maprs7750864
PheGenIrs7750864
hapmaprs7750864
1000 genomesrs7750864
hgdprs7750864
ensemblrs7750864
gopubmedrs7750864
geneviewrs7750864
scholarrs7750864
googlers7750864
pharmgkbrs7750864
gwascentralrs7750864
openSNPrs7750864
23andMers7750864
23andMe allrs7750864
SNP Nexus

SNPshotrs7750864
SNPdbers7750864
MSV3drs7750864
GWAS Ctlgrs7750864
Max Magnitude0
ClinVar
Risk rs7750864(C;C)
Alt rs7750864(C;C)
Reference rs7750864(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31323030T>C
CLNSRC
CLNACC