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rs61759950

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61759950(A;A)
Make rs61759950(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355545
GeneHLA-B
is asnp
is mentioned by
dbSNPrs61759950
ebirs61759950
HLIrs61759950
Exacrs61759950
Varsomers61759950
Maprs61759950
PheGenIrs61759950
hapmaprs61759950
1000 genomesrs61759950
hgdprs61759950
ensemblrs61759950
gopubmedrs61759950
geneviewrs61759950
scholarrs61759950
googlers61759950
pharmgkbrs61759950
gwascentralrs61759950
openSNPrs61759950
23andMers61759950
23andMe allrs61759950
SNP Nexus

SNPshotrs61759950
SNPdbers61759950
MSV3drs61759950
GWAS Ctlgrs61759950
Max Magnitude0
ClinVar
Risk rs61759950(A;A)
Alt rs61759950(A;A)
Reference rs61759950(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323322C>T
CLNSRC
CLNACC