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rs151341398

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341398(-;-)
Make rs151341398(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354449
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341398
ebirs151341398
HLIrs151341398
Exacrs151341398
Varsomers151341398
Maprs151341398
PheGenIrs151341398
hapmaprs151341398
1000 genomesrs151341398
hgdprs151341398
ensemblrs151341398
gopubmedrs151341398
geneviewrs151341398
scholarrs151341398
googlers151341398
pharmgkbrs151341398
gwascentralrs151341398
openSNPrs151341398
23andMers151341398
23andMe allrs151341398
SNP Nexus

SNPshotrs151341398
SNPdbers151341398
MSV3drs151341398
GWAS Ctlgrs151341398
Max Magnitude0
ClinVar
Risk rs151341398(;)
Alt rs151341398(;)
Reference rs151341398(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322226delC
CLNSRC
CLNACC