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rs41542113

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41542113(C;C)
Make rs41542113(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355383
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41542113
ebirs41542113
HLIrs41542113
Exacrs41542113
Varsomers41542113
Maprs41542113
PheGenIrs41542113
hapmaprs41542113
1000 genomesrs41542113
hgdprs41542113
ensemblrs41542113
gopubmedrs41542113
geneviewrs41542113
scholarrs41542113
googlers41542113
pharmgkbrs41542113
gwascentralrs41542113
openSNPrs41542113
23andMers41542113
23andMe allrs41542113
SNP Nexus

SNPshotrs41542113
SNPdbers41542113
MSV3drs41542113
GWAS Ctlgrs41542113
Max Magnitude0
ClinVar
Risk rs41542113(C;C)
Alt rs41542113(C;C)
Reference rs41542113(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323160C>G
CLNSRC
CLNACC