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rs45509993

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45509993(A;A)
Make rs45509993(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356898
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45509993
ebirs45509993
HLIrs45509993
Exacrs45509993
Varsomers45509993
Maprs45509993
PheGenIrs45509993
hapmaprs45509993
1000 genomesrs45509993
hgdprs45509993
ensemblrs45509993
gopubmedrs45509993
geneviewrs45509993
scholarrs45509993
googlers45509993
pharmgkbrs45509993
gwascentralrs45509993
openSNPrs45509993
23andMers45509993
23andMe allrs45509993
SNP Nexus

SNPshotrs45509993
SNPdbers45509993
MSV3drs45509993
GWAS Ctlgrs45509993
Max Magnitude0
ClinVar
Risk rs45509993(A,G,T;A,G,T)
Alt rs45509993(A,G,T;A,G,T)
Reference rs45509993(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324675G>A; NC_000006.11:g.31324675G>C; NC_000006.11:g.31324675G>T
CLNSRC
CLNACC