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rs1050517

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1050517(C;G)
Make rs1050517(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356866
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1050517
dbSNP (classic)rs1050517
ClinGenrs1050517
ebirs1050517
HLIrs1050517
Exacrs1050517
Gnomadrs1050517
Varsomers1050517
LitVarrs1050517
Maprs1050517
PheGenIrs1050517
Biobankrs1050517
1000 genomesrs1050517
hgdprs1050517
ensemblrs1050517
geneviewrs1050517
scholarrs1050517
googlers1050517
pharmgkbrs1050517
gwascentralrs1050517
openSNPrs1050517
23andMers1050517
SNPshotrs1050517
SNPdbers1050517
MSV3drs1050517
GWAS Ctlgrs1050517
GMAF0.3806
Max Magnitude0
ClinVar
Risk rs1050517(A;A) rs1050517(G;G) rs1050517(T;T)
Alt rs1050517(A;A) rs1050517(G;G) rs1050517(T;T)
Reference Rs1050517(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324643G>A; NC_000006.11:g.31324643G>C; NC_000006.11:g.31324643G>T
CLNSRC
CLNACC