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rs151341156

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341156(A;A)
Make rs151341156(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356802
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341156
dbSNP (classic)rs151341156
ClinGenrs151341156
ebirs151341156
HLIrs151341156
Exacrs151341156
Gnomadrs151341156
Varsomers151341156
LitVarrs151341156
Maprs151341156
PheGenIrs151341156
Biobankrs151341156
1000 genomesrs151341156
hgdprs151341156
ensemblrs151341156
geneviewrs151341156
scholarrs151341156
googlers151341156
pharmgkbrs151341156
gwascentralrs151341156
openSNPrs151341156
23andMers151341156
SNPshotrs151341156
SNPdbers151341156
MSV3drs151341156
GWAS Ctlgrs151341156
Max Magnitude0
ClinVar
Risk rs151341156(A;A)
Alt rs151341156(A;A)
Reference Rs151341156(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324579C>T
CLNSRC
CLNACC