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rs137854633

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137854633(-;-)
Make rs137854633(-;A)
Make rs137854633(A;A)
ReferenceGRCh38 38.1/142
Chromosome6
Position31357074
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854633
ebirs137854633
HLIrs137854633
Exacrs137854633
Varsomers137854633
Maprs137854633
PheGenIrs137854633
hapmaprs137854633
1000 genomesrs137854633
hgdprs137854633
ensemblrs137854633
gopubmedrs137854633
geneviewrs137854633
scholarrs137854633
googlers137854633
pharmgkbrs137854633
gwascentralrs137854633
openSNPrs137854633
23andMers137854633
23andMe allrs137854633
SNP Nexus

SNPshotrs137854633
SNPdbers137854633
MSV3drs137854633
GWAS Ctlgrs137854633
Max Magnitude0
ClinVar
Risk rs137854633(AT,GT;AT,GT)
Alt rs137854633(AT,GT;AT,GT)
Reference rs137854633(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324851_31324852insC
CLNSRC
CLNACC