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rs61759951

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61759951(C;C)
Make rs61759951(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355507
GeneHLA-B
is asnp
is mentioned by
dbSNPrs61759951
ebirs61759951
HLIrs61759951
Exacrs61759951
Varsomers61759951
Maprs61759951
PheGenIrs61759951
hapmaprs61759951
1000 genomesrs61759951
hgdprs61759951
ensemblrs61759951
gopubmedrs61759951
geneviewrs61759951
scholarrs61759951
googlers61759951
pharmgkbrs61759951
gwascentralrs61759951
openSNPrs61759951
23andMers61759951
23andMe allrs61759951
SNP Nexus

SNPshotrs61759951
SNPdbers61759951
MSV3drs61759951
GWAS Ctlgrs61759951
Max Magnitude0
ClinVar
Risk rs61759951(C;C)
Alt rs61759951(C;C)
Reference rs61759951(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323284C>G
CLNSRC
CLNACC