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rs41559613

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559613(G;T)
Make rs41559613(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356694
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559613
ebirs41559613
HLIrs41559613
Exacrs41559613
Varsomers41559613
Maprs41559613
PheGenIrs41559613
hapmaprs41559613
1000 genomesrs41559613
hgdprs41559613
ensemblrs41559613
gopubmedrs41559613
geneviewrs41559613
scholarrs41559613
googlers41559613
pharmgkbrs41559613
gwascentralrs41559613
openSNPrs41559613
23andMers41559613
23andMe allrs41559613
SNP Nexus

SNPshotrs41559613
SNPdbers41559613
MSV3drs41559613
GWAS Ctlgrs41559613
Max Magnitude0
ClinVar
Risk rs41559613(A,T;A,T)
Alt rs41559613(A,T;A,T)
Reference rs41559613(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324471C>A; NC_000006.11:g.31324471C>T
CLNSRC
CLNACC