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rs1050529

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050529(A;A)
Make rs1050529(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356838
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1050529
dbSNP (classic)rs1050529
ClinGenrs1050529
ebirs1050529
HLIrs1050529
Exacrs1050529
Gnomadrs1050529
Varsomers1050529
LitVarrs1050529
Maprs1050529
PheGenIrs1050529
Biobankrs1050529
1000 genomesrs1050529
hgdprs1050529
ensemblrs1050529
geneviewrs1050529
scholarrs1050529
googlers1050529
pharmgkbrs1050529
gwascentralrs1050529
openSNPrs1050529
23andMers1050529
SNPshotrs1050529
SNPdbers1050529
MSV3drs1050529
GWAS Ctlgrs1050529
GMAF0.242
Max Magnitude0
ClinVar
Risk rs1050529(A;A)
Alt rs1050529(A;A)
Reference Rs1050529(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324615C>T
CLNSRC
CLNACC