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rs141484466

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141484466(C;C)
Make rs141484466(C;T)
Make rs141484466(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356775
GeneHLA-B
is asnp
is mentioned by
dbSNPrs141484466
ebirs141484466
HLIrs141484466
Exacrs141484466
Varsomers141484466
Maprs141484466
PheGenIrs141484466
hapmaprs141484466
1000 genomesrs141484466
hgdprs141484466
ensemblrs141484466
gopubmedrs141484466
geneviewrs141484466
scholarrs141484466
googlers141484466
pharmgkbrs141484466
gwascentralrs141484466
openSNPrs141484466
23andMers141484466
23andMe allrs141484466
SNP Nexus

SNPshotrs141484466
SNPdbers141484466
MSV3drs141484466
GWAS Ctlgrs141484466
Merged fromRs151341169
Max Magnitude0
ClinVar
Risk rs141484466(A,C;A,C)
Alt rs141484466(A,C;A,C)
Reference rs141484466(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324552G>A; NC_000006.11:g.31324552G>C
CLNSRC
CLNACC