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rs41559115

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559115(C;C)
Make rs41559115(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356542
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559115
ebirs41559115
HLIrs41559115
Exacrs41559115
Varsomers41559115
Maprs41559115
PheGenIrs41559115
hapmaprs41559115
1000 genomesrs41559115
hgdprs41559115
ensemblrs41559115
gopubmedrs41559115
geneviewrs41559115
scholarrs41559115
googlers41559115
pharmgkbrs41559115
gwascentralrs41559115
openSNPrs41559115
23andMers41559115
23andMe allrs41559115
SNP Nexus

SNPshotrs41559115
SNPdbers41559115
MSV3drs41559115
GWAS Ctlgrs41559115
Max Magnitude0
ClinVar
Risk rs41559115(C;C)
Alt rs41559115(C;C)
Reference rs41559115(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324319C>G
CLNSRC
CLNACC