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rs137854644

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137854644(A;A)
Make rs137854644(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356924
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854644
ebirs137854644
HLIrs137854644
Exacrs137854644
Varsomers137854644
Maprs137854644
PheGenIrs137854644
hapmaprs137854644
1000 genomesrs137854644
hgdprs137854644
ensemblrs137854644
gopubmedrs137854644
geneviewrs137854644
scholarrs137854644
googlers137854644
pharmgkbrs137854644
gwascentralrs137854644
openSNPrs137854644
23andMers137854644
23andMe allrs137854644
SNP Nexus

SNPshotrs137854644
SNPdbers137854644
MSV3drs137854644
GWAS Ctlgrs137854644
Max Magnitude0
ClinVar
Risk rs137854644(A,C;A,C)
Alt rs137854644(A,C;A,C)
Reference rs137854644(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324701A>G; NC_000006.11:g.31324701A>T
CLNSRC
CLNACC