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rs41552422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41552422(C;T)
Make rs41552422(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354752
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552422
ebirs41552422
HLIrs41552422
Exacrs41552422
Varsomers41552422
Maprs41552422
PheGenIrs41552422
hapmaprs41552422
1000 genomesrs41552422
hgdprs41552422
ensemblrs41552422
gopubmedrs41552422
geneviewrs41552422
scholarrs41552422
googlers41552422
pharmgkbrs41552422
gwascentralrs41552422
openSNPrs41552422
23andMers41552422
23andMe allrs41552422
SNP Nexus

SNPshotrs41552422
SNPdbers41552422
MSV3drs41552422
GWAS Ctlgrs41552422
Max Magnitude0
ClinVar
Risk rs41552422(T;T)
Alt rs41552422(T;T)
Reference rs41552422(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322529G>A
CLNSRC
CLNACC