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rs151341303

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341303(A;A)
Make rs151341303(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356255
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341303
ebirs151341303
HLIrs151341303
Exacrs151341303
Varsomers151341303
Maprs151341303
PheGenIrs151341303
hapmaprs151341303
1000 genomesrs151341303
hgdprs151341303
ensemblrs151341303
gopubmedrs151341303
geneviewrs151341303
scholarrs151341303
googlers151341303
pharmgkbrs151341303
gwascentralrs151341303
openSNPrs151341303
23andMers151341303
23andMe allrs151341303
SNP Nexus

SNPshotrs151341303
SNPdbers151341303
MSV3drs151341303
GWAS Ctlgrs151341303
Merged fromRs151341304, Rs151341305
Max Magnitude0
ClinVar
Risk rs151341303(A,C,T;A,C,T)
Alt rs151341303(A,C,T;A,C,T)
Reference rs151341303(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324032C>A; NC_000006.11:g.31324032C>G; NC_000006.11:g.31324032C>T
CLNSRC
CLNACC