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rs144857500

From SNPedia

Merged intors1050543
Orientationminus
Stabilizedplus
Make rs144857500(C;C)
Make rs144857500(C;G)
Make rs144857500(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356818
GeneHLA-B
is asnp
is mentioned by
dbSNPrs144857500
ebirs144857500
HLIrs144857500
Exacrs144857500
Varsomers144857500
Maprs144857500
PheGenIrs144857500
hapmaprs144857500
1000 genomesrs144857500
hgdprs144857500
ensemblrs144857500
gopubmedrs144857500
geneviewrs144857500
scholarrs144857500
googlers144857500
pharmgkbrs144857500
gwascentralrs144857500
openSNPrs144857500
23andMers144857500
23andMe allrs144857500
SNP Nexus

SNPshotrs144857500
SNPdbers144857500
MSV3drs144857500
GWAS Ctlgrs144857500
StatusMerged into rs1050543
Max Magnitude
ClinVar
Risk rs144857500(G;G)
Alt rs144857500(G;G)
Reference rs144857500(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324595C>G
CLNSRC
CLNACC