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rs61759953

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61759953(A;C)
Make rs61759953(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355458
GeneHLA-B
is asnp
is mentioned by
dbSNPrs61759953
ebirs61759953
HLIrs61759953
Exacrs61759953
Varsomers61759953
Maprs61759953
PheGenIrs61759953
hapmaprs61759953
1000 genomesrs61759953
hgdprs61759953
ensemblrs61759953
gopubmedrs61759953
geneviewrs61759953
scholarrs61759953
googlers61759953
pharmgkbrs61759953
gwascentralrs61759953
openSNPrs61759953
23andMers61759953
23andMe allrs61759953
SNP Nexus

SNPshotrs61759953
SNPdbers61759953
MSV3drs61759953
GWAS Ctlgrs61759953
Max Magnitude0
ClinVar
Risk rs61759953(C,G,T;C,G,T)
Alt rs61759953(C,G,T;C,G,T)
Reference rs61759953(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323235T>A; NC_000006.11:g.31323235T>C; NC_000006.11:g.31323235T>G
CLNSRC
CLNACC