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rs41563536

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41563536(C;G)
Make rs41563536(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356789
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41563536
ebirs41563536
HLIrs41563536
Exacrs41563536
Varsomers41563536
Maprs41563536
PheGenIrs41563536
hapmaprs41563536
1000 genomesrs41563536
hgdprs41563536
ensemblrs41563536
gopubmedrs41563536
geneviewrs41563536
scholarrs41563536
googlers41563536
pharmgkbrs41563536
gwascentralrs41563536
openSNPrs41563536
23andMers41563536
23andMe allrs41563536
SNP Nexus

SNPshotrs41563536
SNPdbers41563536
MSV3drs41563536
GWAS Ctlgrs41563536
Max Magnitude0
ClinVar
Risk rs41563536(G,T;G,T)
Alt rs41563536(G,T;G,T)
Reference rs41563536(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324566G>A; NC_000006.11:g.31324566G>C
CLNSRC
CLNACC