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rs41542712

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41542712(C;G)
Make rs41542712(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356241
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41542712
ebirs41542712
HLIrs41542712
Exacrs41542712
Varsomers41542712
Maprs41542712
PheGenIrs41542712
hapmaprs41542712
1000 genomesrs41542712
hgdprs41542712
ensemblrs41542712
gopubmedrs41542712
geneviewrs41542712
scholarrs41542712
googlers41542712
pharmgkbrs41542712
gwascentralrs41542712
openSNPrs41542712
23andMers41542712
23andMe allrs41542712
SNP Nexus

SNPshotrs41542712
SNPdbers41542712
MSV3drs41542712
GWAS Ctlgrs41542712
Max Magnitude0
ClinVar
Risk rs41542712(G,T;G,T)
Alt rs41542712(G,T;G,T)
Reference rs41542712(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324018G>A; NC_000006.11:g.31324018G>C
CLNSRC
CLNACC