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rs151341158

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341158(A;A)
Make rs151341158(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356800
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341158
dbSNP (classic)rs151341158
ClinGenrs151341158
ebirs151341158
HLIrs151341158
Exacrs151341158
Gnomadrs151341158
Varsomers151341158
LitVarrs151341158
Maprs151341158
PheGenIrs151341158
Biobankrs151341158
1000 genomesrs151341158
hgdprs151341158
ensemblrs151341158
geneviewrs151341158
scholarrs151341158
googlers151341158
pharmgkbrs151341158
gwascentralrs151341158
openSNPrs151341158
23andMers151341158
SNPshotrs151341158
SNPdbers151341158
MSV3drs151341158
GWAS Ctlgrs151341158
Max Magnitude0
ClinVar
Risk rs151341158(A;A) rs151341158(C;C)
Alt rs151341158(A;A) rs151341158(C;C)
Reference Rs151341158(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324577C>G; NC_000006.11:g.31324577C>T
CLNSRC
CLNACC