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rs61759949

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61759949(A;G)
Make rs61759949(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356193
GeneHLA-B
is asnp
is mentioned by
dbSNPrs61759949
ebirs61759949
HLIrs61759949
Exacrs61759949
Varsomers61759949
Maprs61759949
PheGenIrs61759949
hapmaprs61759949
1000 genomesrs61759949
hgdprs61759949
ensemblrs61759949
gopubmedrs61759949
geneviewrs61759949
scholarrs61759949
googlers61759949
pharmgkbrs61759949
gwascentralrs61759949
openSNPrs61759949
23andMers61759949
23andMe allrs61759949
SNP Nexus

SNPshotrs61759949
SNPdbers61759949
MSV3drs61759949
GWAS Ctlgrs61759949
Max Magnitude0
ClinVar
Risk rs61759949(C,G,T;C,G,T)
Alt rs61759949(C,G,T;C,G,T)
Reference rs61759949(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323970T>C
CLNSRC
CLNACC