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rs61759955

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61759955(C;C)
Make rs61759955(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354901
GeneHLA-B
is asnp
is mentioned by
dbSNPrs61759955
ebirs61759955
HLIrs61759955
Exacrs61759955
Varsomers61759955
Maprs61759955
PheGenIrs61759955
hapmaprs61759955
1000 genomesrs61759955
hgdprs61759955
ensemblrs61759955
gopubmedrs61759955
geneviewrs61759955
scholarrs61759955
googlers61759955
pharmgkbrs61759955
gwascentralrs61759955
openSNPrs61759955
23andMers61759955
23andMe allrs61759955
SNP Nexus

SNPshotrs61759955
SNPdbers61759955
MSV3drs61759955
GWAS Ctlgrs61759955
Max Magnitude0
ClinVar
Risk rs61759955(C;C)
Alt rs61759955(C;C)
Reference rs61759955(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322678A>G
CLNSRC
CLNACC