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rs61759954

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61759954(A;A)
Make rs61759954(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355149
GeneHLA-B
is asnp
is mentioned by
dbSNPrs61759954
ebirs61759954
HLIrs61759954
Exacrs61759954
Varsomers61759954
Maprs61759954
PheGenIrs61759954
hapmaprs61759954
1000 genomesrs61759954
hgdprs61759954
ensemblrs61759954
gopubmedrs61759954
geneviewrs61759954
scholarrs61759954
googlers61759954
pharmgkbrs61759954
gwascentralrs61759954
openSNPrs61759954
23andMers61759954
23andMe allrs61759954
SNP Nexus

SNPshotrs61759954
SNPdbers61759954
MSV3drs61759954
GWAS Ctlgrs61759954
Max Magnitude0
ClinVar
Risk rs61759954(A;A)
Alt rs61759954(A;A)
Reference rs61759954(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322926C>T
CLNSRC
CLNACC