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rs41559413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559413(C;C)
Make rs41559413(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356559
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559413
ebirs41559413
HLIrs41559413
Exacrs41559413
Varsomers41559413
Maprs41559413
PheGenIrs41559413
hapmaprs41559413
1000 genomesrs41559413
hgdprs41559413
ensemblrs41559413
gopubmedrs41559413
geneviewrs41559413
scholarrs41559413
googlers41559413
pharmgkbrs41559413
gwascentralrs41559413
openSNPrs41559413
23andMers41559413
23andMe allrs41559413
SNP Nexus

SNPshotrs41559413
SNPdbers41559413
MSV3drs41559413
GWAS Ctlgrs41559413
Max Magnitude0
ClinVar
Risk rs41559413(C;C)
Alt rs41559413(C;C)
Reference rs41559413(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324336C>G
CLNSRC
CLNACC