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rs41563212

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41563212(C;C)
Make rs41563212(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355868
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41563212
ebirs41563212
HLIrs41563212
Exacrs41563212
Varsomers41563212
Maprs41563212
PheGenIrs41563212
hapmaprs41563212
1000 genomesrs41563212
hgdprs41563212
ensemblrs41563212
gopubmedrs41563212
geneviewrs41563212
scholarrs41563212
googlers41563212
pharmgkbrs41563212
gwascentralrs41563212
openSNPrs41563212
23andMers41563212
23andMe allrs41563212
SNP Nexus

SNPshotrs41563212
SNPdbers41563212
MSV3drs41563212
GWAS Ctlgrs41563212
Max Magnitude0
ClinVar
Risk rs41563212(C;C)
Alt rs41563212(C;C)
Reference rs41563212(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323645A>G
CLNSRC
CLNACC