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rs151341326

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341326(A;A)
Make rs151341326(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356195
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341326
dbSNP (classic)rs151341326
ClinGenrs151341326
ebirs151341326
HLIrs151341326
Exacrs151341326
Gnomadrs151341326
Varsomers151341326
LitVarrs151341326
Maprs151341326
PheGenIrs151341326
Biobankrs151341326
1000 genomesrs151341326
hgdprs151341326
ensemblrs151341326
geneviewrs151341326
scholarrs151341326
googlers151341326
pharmgkbrs151341326
gwascentralrs151341326
openSNPrs151341326
23andMers151341326
SNPshotrs151341326
SNPdbers151341326
MSV3drs151341326
GWAS Ctlgrs151341326
Max Magnitude0
ClinVar
Risk rs151341326(A;A)
Alt rs151341326(A;A)
Reference Rs151341326(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323972C>T
CLNSRC
CLNACC