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rs151341360

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341360(G;T)
Make rs151341360(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355373
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341360
dbSNP (classic)rs151341360
ClinGenrs151341360
ebirs151341360
HLIrs151341360
Exacrs151341360
Gnomadrs151341360
Varsomers151341360
LitVarrs151341360
Maprs151341360
PheGenIrs151341360
Biobankrs151341360
1000 genomesrs151341360
hgdprs151341360
ensemblrs151341360
geneviewrs151341360
scholarrs151341360
googlers151341360
pharmgkbrs151341360
gwascentralrs151341360
openSNPrs151341360
23andMers151341360
SNPshotrs151341360
SNPdbers151341360
MSV3drs151341360
GWAS Ctlgrs151341360
Max Magnitude0
ClinVar
Risk rs151341360(T;T)
Alt rs151341360(T;T)
Reference Rs151341360(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323150C>A
CLNSRC
CLNACC