Have questions? Visit https://www.reddit.com/r/SNPedia

rs1065502

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1065502(A;A)
Make rs1065502(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355378
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs1065502
dbSNP (classic)rs1065502
ClinGenrs1065502
ebirs1065502
HLIrs1065502
Exacrs1065502
Gnomadrs1065502
Varsomers1065502
LitVarrs1065502
Maprs1065502
PheGenIrs1065502
Biobankrs1065502
1000 genomesrs1065502
hgdprs1065502
ensemblrs1065502
geneviewrs1065502
scholarrs1065502
googlers1065502
pharmgkbrs1065502
gwascentralrs1065502
openSNPrs1065502
23andMers1065502
SNPshotrs1065502
SNPdbers1065502
MSV3drs1065502
GWAS Ctlgrs1065502
Max Magnitude0
ClinVar
Risk rs1065502(A;A)
Alt rs1065502(A;A)
Reference Rs1065502(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323155C>T
CLNSRC
CLNACC