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rs151341102

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341102(G;T)
Make rs151341102(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356909
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341102
dbSNP (classic)rs151341102
ClinGenrs151341102
ebirs151341102
HLIrs151341102
Exacrs151341102
Gnomadrs151341102
Varsomers151341102
LitVarrs151341102
Maprs151341102
PheGenIrs151341102
Biobankrs151341102
1000 genomesrs151341102
hgdprs151341102
ensemblrs151341102
geneviewrs151341102
scholarrs151341102
googlers151341102
pharmgkbrs151341102
gwascentralrs151341102
openSNPrs151341102
23andMers151341102
SNPshotrs151341102
SNPdbers151341102
MSV3drs151341102
GWAS Ctlgrs151341102
Max Magnitude0
ClinVar
Risk rs151341102(T;T)
Alt rs151341102(T;T)
Reference Rs151341102(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324686C>A
CLNSRC
CLNACC