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rs151341227

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341227(A;A)
Make rs151341227(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356400
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341227
dbSNP (classic)rs151341227
ClinGenrs151341227
ebirs151341227
HLIrs151341227
Exacrs151341227
Gnomadrs151341227
Varsomers151341227
LitVarrs151341227
Maprs151341227
PheGenIrs151341227
Biobankrs151341227
1000 genomesrs151341227
hgdprs151341227
ensemblrs151341227
geneviewrs151341227
scholarrs151341227
googlers151341227
pharmgkbrs151341227
gwascentralrs151341227
openSNPrs151341227
23andMers151341227
SNPshotrs151341227
SNPdbers151341227
MSV3drs151341227
GWAS Ctlgrs151341227
Max Magnitude0
ClinVar
Risk rs151341227(A;A)
Alt rs151341227(A;A)
Reference Rs151341227(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324177G>T
CLNSRC
CLNACC