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rs41544018

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41544018(-;-)
Make rs41544018(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324090
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41544018
ebirs41544018
HLIrs41544018
Exacrs41544018
Varsomers41544018
Maprs41544018
PheGenIrs41544018
hapmaprs41544018
1000 genomesrs41544018
hgdprs41544018
ensemblrs41544018
gopubmedrs41544018
geneviewrs41544018
scholarrs41544018
googlers41544018
pharmgkbrs41544018
gwascentralrs41544018
openSNPrs41544018
23andMers41544018
23andMe allrs41544018
SNP Nexus

SNPshotrs41544018
SNPdbers41544018
MSV3drs41544018
GWAS Ctlgrs41544018
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41544018(;)
Alt rs41544018(;)
Reference rs41544018(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324090delG
CLNSRC
CLNACC