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rs137854679

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854679(A;A)
Make rs137854679(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356779
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854679
ebirs137854679
HLIrs137854679
Exacrs137854679
Varsomers137854679
Maprs137854679
PheGenIrs137854679
hapmaprs137854679
1000 genomesrs137854679
hgdprs137854679
ensemblrs137854679
gopubmedrs137854679
geneviewrs137854679
scholarrs137854679
googlers137854679
pharmgkbrs137854679
gwascentralrs137854679
openSNPrs137854679
23andMers137854679
23andMe allrs137854679
SNP Nexus

SNPshotrs137854679
SNPdbers137854679
MSV3drs137854679
GWAS Ctlgrs137854679
Max Magnitude0
ClinVar
Risk rs137854679(A,C;A,C)
Alt rs137854679(A,C;A,C)
Reference rs137854679(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324556C>G; NC_000006.11:g.31324556C>T
CLNSRC
CLNACC