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rs41548516

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41548516(G;T)
Make rs41548516(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355148
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41548516
ebirs41548516
HLIrs41548516
Exacrs41548516
Varsomers41548516
Maprs41548516
PheGenIrs41548516
hapmaprs41548516
1000 genomesrs41548516
hgdprs41548516
ensemblrs41548516
gopubmedrs41548516
geneviewrs41548516
scholarrs41548516
googlers41548516
pharmgkbrs41548516
gwascentralrs41548516
openSNPrs41548516
23andMers41548516
23andMe allrs41548516
SNP Nexus

SNPshotrs41548516
SNPdbers41548516
MSV3drs41548516
GWAS Ctlgrs41548516
Max Magnitude0
ClinVar
Risk rs41548516(T;T)
Alt rs41548516(T;T)
Reference rs41548516(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322925C>A
CLNSRC
CLNACC