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rs41559014

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41559014(C;C)
Make rs41559014(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356325
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559014
ebirs41559014
HLIrs41559014
Exacrs41559014
Varsomers41559014
Maprs41559014
PheGenIrs41559014
hapmaprs41559014
1000 genomesrs41559014
hgdprs41559014
ensemblrs41559014
gopubmedrs41559014
geneviewrs41559014
scholarrs41559014
googlers41559014
pharmgkbrs41559014
gwascentralrs41559014
openSNPrs41559014
23andMers41559014
23andMe allrs41559014
SNP Nexus

SNPshotrs41559014
SNPdbers41559014
MSV3drs41559014
GWAS Ctlgrs41559014
Max Magnitude0
ClinVar
Risk rs41559014(A,C;A,C)
Alt rs41559014(A,C;A,C)
Reference rs41559014(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324102A>G; NC_000006.11:g.31324102A>T
CLNSRC
CLNACC