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rs151341226

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341226(C;C)
Make rs151341226(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356404
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341226
dbSNP (classic)rs151341226
ClinGenrs151341226
ebirs151341226
HLIrs151341226
Exacrs151341226
Gnomadrs151341226
Varsomers151341226
LitVarrs151341226
Maprs151341226
PheGenIrs151341226
Biobankrs151341226
1000 genomesrs151341226
hgdprs151341226
ensemblrs151341226
geneviewrs151341226
scholarrs151341226
googlers151341226
pharmgkbrs151341226
gwascentralrs151341226
openSNPrs151341226
23andMers151341226
SNPshotrs151341226
SNPdbers151341226
MSV3drs151341226
GWAS Ctlgrs151341226
Max Magnitude0
ClinVar
Risk rs151341226(C;C)
Alt rs151341226(C;C)
Reference Rs151341226(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324181C>G
CLNSRC
CLNACC