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rs41553920

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41553920(-;-)
Make rs41553920(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324541
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41553920
ebirs41553920
HLIrs41553920
Exacrs41553920
Varsomers41553920
Maprs41553920
PheGenIrs41553920
hapmaprs41553920
1000 genomesrs41553920
hgdprs41553920
ensemblrs41553920
gopubmedrs41553920
geneviewrs41553920
scholarrs41553920
googlers41553920
pharmgkbrs41553920
gwascentralrs41553920
openSNPrs41553920
23andMers41553920
23andMe allrs41553920
SNP Nexus

SNPshotrs41553920
SNPdbers41553920
MSV3drs41553920
GWAS Ctlgrs41553920
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41553920(;)
Alt rs41553920(;)
Reference rs41553920(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324541delC
CLNSRC
CLNACC