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rs1065378

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1065378(A;C)
Make rs1065378(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356856
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1065378
ebirs1065378
HLIrs1065378
Exacrs1065378
Varsomers1065378
Maprs1065378
PheGenIrs1065378
hapmaprs1065378
1000 genomesrs1065378
hgdprs1065378
ensemblrs1065378
gopubmedrs1065378
geneviewrs1065378
scholarrs1065378
googlers1065378
pharmgkbrs1065378
gwascentralrs1065378
openSNPrs1065378
23andMers1065378
23andMe allrs1065378
SNP Nexus

SNPshotrs1065378
SNPdbers1065378
MSV3drs1065378
GWAS Ctlgrs1065378
Max Magnitude0
ClinVar
Risk rs1065378(C,G;C,G)
Alt rs1065378(C,G;C,G)
Reference rs1065378(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324633T>C; NC_000006.11:g.31324633T>G
CLNSRC
CLNACC