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rs41544413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41544413(C;T)
Make rs41544413(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356848
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41544413
ebirs41544413
HLIrs41544413
Exacrs41544413
Varsomers41544413
Maprs41544413
PheGenIrs41544413
hapmaprs41544413
1000 genomesrs41544413
hgdprs41544413
ensemblrs41544413
gopubmedrs41544413
geneviewrs41544413
scholarrs41544413
googlers41544413
pharmgkbrs41544413
gwascentralrs41544413
openSNPrs41544413
23andMers41544413
23andMe allrs41544413
SNP Nexus

SNPshotrs41544413
SNPdbers41544413
MSV3drs41544413
GWAS Ctlgrs41544413
Max Magnitude0
ClinVar
Risk rs41544413(T;T)
Alt rs41544413(T;T)
Reference rs41544413(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324625G>A
CLNSRC
CLNACC