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rs41558317

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41558317(C;C)
Make rs41558317(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355073
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41558317
ebirs41558317
HLIrs41558317
Exacrs41558317
Varsomers41558317
Maprs41558317
PheGenIrs41558317
hapmaprs41558317
1000 genomesrs41558317
hgdprs41558317
ensemblrs41558317
gopubmedrs41558317
geneviewrs41558317
scholarrs41558317
googlers41558317
pharmgkbrs41558317
gwascentralrs41558317
openSNPrs41558317
23andMers41558317
23andMe allrs41558317
SNP Nexus

SNPshotrs41558317
SNPdbers41558317
MSV3drs41558317
GWAS Ctlgrs41558317
Max Magnitude0
ClinVar
Risk rs41558317(C;C)
Alt rs41558317(C;C)
Reference rs41558317(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322850A>G
CLNSRC
CLNACC