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rs137854752

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854752(A;A)
Make rs137854752(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356272
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854752
ebirs137854752
HLIrs137854752
Exacrs137854752
Varsomers137854752
Maprs137854752
PheGenIrs137854752
hapmaprs137854752
1000 genomesrs137854752
hgdprs137854752
ensemblrs137854752
gopubmedrs137854752
geneviewrs137854752
scholarrs137854752
googlers137854752
pharmgkbrs137854752
gwascentralrs137854752
openSNPrs137854752
23andMers137854752
23andMe allrs137854752
SNP Nexus

SNPshotrs137854752
SNPdbers137854752
MSV3drs137854752
GWAS Ctlgrs137854752
Max Magnitude0
ClinVar
Risk rs137854752(A,C;A,C)
Alt rs137854752(A,C;A,C)
Reference rs137854752(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324049C>G; NC_000006.11:g.31324049C>T
CLNSRC
CLNACC