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rs41556315

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41556315(G;T)
Make rs41556315(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355949
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556315
ebirs41556315
HLIrs41556315
Exacrs41556315
Varsomers41556315
Maprs41556315
PheGenIrs41556315
hapmaprs41556315
1000 genomesrs41556315
hgdprs41556315
ensemblrs41556315
gopubmedrs41556315
geneviewrs41556315
scholarrs41556315
googlers41556315
pharmgkbrs41556315
gwascentralrs41556315
openSNPrs41556315
23andMers41556315
23andMe allrs41556315
SNP Nexus

SNPshotrs41556315
SNPdbers41556315
MSV3drs41556315
GWAS Ctlgrs41556315
Max Magnitude0
ClinVar
Risk rs41556315(T;T)
Alt rs41556315(T;T)
Reference rs41556315(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323726C>A
CLNSRC
CLNACC