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rs61759947

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61759947(A;A)
Make rs61759947(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356398
GeneHLA-B
is asnp
is mentioned by
dbSNPrs61759947
ebirs61759947
HLIrs61759947
Exacrs61759947
Varsomers61759947
Maprs61759947
PheGenIrs61759947
hapmaprs61759947
1000 genomesrs61759947
hgdprs61759947
ensemblrs61759947
gopubmedrs61759947
geneviewrs61759947
scholarrs61759947
googlers61759947
pharmgkbrs61759947
gwascentralrs61759947
openSNPrs61759947
23andMers61759947
23andMe allrs61759947
SNP Nexus

SNPshotrs61759947
SNPdbers61759947
MSV3drs61759947
GWAS Ctlgrs61759947
Max Magnitude0
ClinVar
Risk rs61759947(A,C,T;A,C,T)
Alt rs61759947(A,C,T;A,C,T)
Reference rs61759947(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324175C>A; NC_000006.11:g.31324175C>G; NC_000006.11:g.31324175C>T
CLNSRC
CLNACC