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rs151341297

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341297(A;A)
Make rs151341297(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356258
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341297
ebirs151341297
HLIrs151341297
Exacrs151341297
Varsomers151341297
Maprs151341297
PheGenIrs151341297
hapmaprs151341297
1000 genomesrs151341297
hgdprs151341297
ensemblrs151341297
gopubmedrs151341297
geneviewrs151341297
scholarrs151341297
googlers151341297
pharmgkbrs151341297
gwascentralrs151341297
openSNPrs151341297
23andMers151341297
23andMe allrs151341297
SNP Nexus

SNPshotrs151341297
SNPdbers151341297
MSV3drs151341297
GWAS Ctlgrs151341297
Merged fromRs151341298, Rs151341299
Max Magnitude0
ClinVar
Risk rs151341297(A,C,T;A,C,T)
Alt rs151341297(A,C,T;A,C,T)
Reference rs151341297(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324035C>A; NC_000006.11:g.31324035C>G; NC_000006.11:g.31324035C>T
CLNSRC
CLNACC