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rs151341397

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341397(A;A)
Make rs151341397(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354451
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341397
ebirs151341397
HLIrs151341397
Exacrs151341397
Varsomers151341397
Maprs151341397
PheGenIrs151341397
hapmaprs151341397
1000 genomesrs151341397
hgdprs151341397
ensemblrs151341397
gopubmedrs151341397
geneviewrs151341397
scholarrs151341397
googlers151341397
pharmgkbrs151341397
gwascentralrs151341397
openSNPrs151341397
23andMers151341397
23andMe allrs151341397
SNP Nexus

SNPshotrs151341397
SNPdbers151341397
MSV3drs151341397
GWAS Ctlgrs151341397
Max Magnitude0
ClinVar
Risk rs151341397(A;A)
Alt rs151341397(A;A)
Reference rs151341397(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322228C>T
CLNSRC
CLNACC