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rs41546313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41546313(C;G)
Make rs41546313(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356753
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41546313
ebirs41546313
HLIrs41546313
Exacrs41546313
Varsomers41546313
Maprs41546313
PheGenIrs41546313
hapmaprs41546313
1000 genomesrs41546313
hgdprs41546313
ensemblrs41546313
gopubmedrs41546313
geneviewrs41546313
scholarrs41546313
googlers41546313
pharmgkbrs41546313
gwascentralrs41546313
openSNPrs41546313
23andMers41546313
23andMe allrs41546313
SNP Nexus

SNPshotrs41546313
SNPdbers41546313
MSV3drs41546313
GWAS Ctlgrs41546313
Max Magnitude0
ClinVar
Risk rs41546313(G,T;G,T)
Alt rs41546313(G,T;G,T)
Reference rs41546313(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324530G>A; NC_000006.11:g.31324530G>C
CLNSRC
CLNACC