Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341255

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341255(A;A)
Make rs151341255(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356308
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341255
dbSNP (classic)rs151341255
ClinGenrs151341255
ebirs151341255
HLIrs151341255
Exacrs151341255
Gnomadrs151341255
Varsomers151341255
LitVarrs151341255
Maprs151341255
PheGenIrs151341255
Biobankrs151341255
1000 genomesrs151341255
hgdprs151341255
ensemblrs151341255
geneviewrs151341255
scholarrs151341255
googlers151341255
pharmgkbrs151341255
gwascentralrs151341255
openSNPrs151341255
23andMers151341255
SNPshotrs151341255
SNPdbers151341255
MSV3drs151341255
GWAS Ctlgrs151341255
Max Magnitude0
ClinVar
Risk rs151341255(A;A)
Alt rs151341255(A;A)
Reference Rs151341255(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324085C>T
CLNSRC
CLNACC