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rs41560522

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41560522(G;T)
Make rs41560522(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356987
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560522
ebirs41560522
HLIrs41560522
Exacrs41560522
Varsomers41560522
Maprs41560522
PheGenIrs41560522
hapmaprs41560522
1000 genomesrs41560522
hgdprs41560522
ensemblrs41560522
gopubmedrs41560522
geneviewrs41560522
scholarrs41560522
googlers41560522
pharmgkbrs41560522
gwascentralrs41560522
openSNPrs41560522
23andMers41560522
23andMe allrs41560522
SNP Nexus

SNPshotrs41560522
SNPdbers41560522
MSV3drs41560522
GWAS Ctlgrs41560522
GMAF0.06061
Max Magnitude0
ClinVar
Risk rs41560522(T;T)
Alt rs41560522(T;T)
Reference rs41560522(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324764C>A
CLNSRC
CLNACC