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rs137854661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854661(A;A)
Make rs137854661(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356871
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854661
ebirs137854661
HLIrs137854661
Exacrs137854661
Varsomers137854661
Maprs137854661
PheGenIrs137854661
hapmaprs137854661
1000 genomesrs137854661
hgdprs137854661
ensemblrs137854661
gopubmedrs137854661
geneviewrs137854661
scholarrs137854661
googlers137854661
pharmgkbrs137854661
gwascentralrs137854661
openSNPrs137854661
23andMers137854661
23andMe allrs137854661
SNP Nexus

SNPshotrs137854661
SNPdbers137854661
MSV3drs137854661
GWAS Ctlgrs137854661
Max Magnitude0
ClinVar
Risk rs137854661(A,T;A,T)
Alt rs137854661(A,T;A,T)
Reference rs137854661(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324648C>A; NC_000006.11:g.31324648C>T
CLNSRC
CLNACC