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

rs151341238

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341238(A;G)
Make rs151341238(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356376
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341238
dbSNP (classic)rs151341238
ClinGenrs151341238
ebirs151341238
HLIrs151341238
Exacrs151341238
Gnomadrs151341238
Varsomers151341238
LitVarrs151341238
Maprs151341238
PheGenIrs151341238
Biobankrs151341238
1000 genomesrs151341238
hgdprs151341238
ensemblrs151341238
geneviewrs151341238
scholarrs151341238
googlers151341238
pharmgkbrs151341238
gwascentralrs151341238
openSNPrs151341238
23andMers151341238
SNPshotrs151341238
SNPdbers151341238
MSV3drs151341238
GWAS Ctlgrs151341238
Max Magnitude0
ClinVar
Risk rs151341238(G;G)
Alt rs151341238(G;G)
Reference Rs151341238(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324153T>C
CLNSRC
CLNACC