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rs151341312

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341312(-;-)
Make rs151341312(-;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356239
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341312
dbSNP (classic)rs151341312
ClinGenrs151341312
ebirs151341312
HLIrs151341312
Exacrs151341312
Gnomadrs151341312
Varsomers151341312
LitVarrs151341312
Maprs151341312
PheGenIrs151341312
Biobankrs151341312
1000 genomesrs151341312
hgdprs151341312
ensemblrs151341312
geneviewrs151341312
scholarrs151341312
googlers151341312
pharmgkbrs151341312
gwascentralrs151341312
openSNPrs151341312
23andMers151341312
SNPshotrs151341312
SNPdbers151341312
MSV3drs151341312
GWAS Ctlgrs151341312
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341312(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324016delA
CLNSRC
CLNACC