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rs151341225

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341225(C;C)
Make rs151341225(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356405
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341225
dbSNP (classic)rs151341225
ClinGenrs151341225
ebirs151341225
HLIrs151341225
Exacrs151341225
Gnomadrs151341225
Varsomers151341225
LitVarrs151341225
Maprs151341225
PheGenIrs151341225
Biobankrs151341225
1000 genomesrs151341225
hgdprs151341225
ensemblrs151341225
geneviewrs151341225
scholarrs151341225
googlers151341225
pharmgkbrs151341225
gwascentralrs151341225
openSNPrs151341225
23andMers151341225
SNPshotrs151341225
SNPdbers151341225
MSV3drs151341225
GWAS Ctlgrs151341225
Max Magnitude0
ClinVar
Risk rs151341225(C;C)
Alt rs151341225(C;C)
Reference Rs151341225(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324182C>G
CLNSRC
CLNACC