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rs41557920

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41557920(-;-)
Make rs41557920(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324028
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41557920
ebirs41557920
HLIrs41557920
Exacrs41557920
Varsomers41557920
Maprs41557920
PheGenIrs41557920
hapmaprs41557920
1000 genomesrs41557920
hgdprs41557920
ensemblrs41557920
gopubmedrs41557920
geneviewrs41557920
scholarrs41557920
googlers41557920
pharmgkbrs41557920
gwascentralrs41557920
openSNPrs41557920
23andMers41557920
23andMe allrs41557920
SNP Nexus

SNPshotrs41557920
SNPdbers41557920
MSV3drs41557920
GWAS Ctlgrs41557920
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41557920(;)
Alt rs41557920(;)
Reference rs41557920(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324028delG
CLNSRC
CLNACC