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rs151341085

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341085(A;A)
Make rs151341085(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356960
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341085
dbSNP (old)rs151341085
ClinGenrs151341085
ebirs151341085
HLIrs151341085
Exacrs151341085
Gnomadrs151341085
Varsomers151341085
Maprs151341085
PheGenIrs151341085
Biobankrs151341085
1000 genomesrs151341085
hgdprs151341085
ensemblrs151341085
gopubmedrs151341085
geneviewrs151341085
scholarrs151341085
googlers151341085
pharmgkbrs151341085
gwascentralrs151341085
openSNPrs151341085
23andMers151341085
23andMe allrs151341085
SNP Nexus

SNPshotrs151341085
SNPdbers151341085
MSV3drs151341085
GWAS Ctlgrs151341085
Max Magnitude0
ClinVar
Risk rs151341085(A;A)
Alt rs151341085(A;A)
Reference Rs151341085(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324737G>T
CLNSRC
CLNACC