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rs41556312

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41556312(G;G)
Make rs41556312(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356430
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556312
ebirs41556312
HLIrs41556312
Exacrs41556312
Varsomers41556312
Maprs41556312
PheGenIrs41556312
hapmaprs41556312
1000 genomesrs41556312
hgdprs41556312
ensemblrs41556312
gopubmedrs41556312
geneviewrs41556312
scholarrs41556312
googlers41556312
pharmgkbrs41556312
gwascentralrs41556312
openSNPrs41556312
23andMers41556312
23andMe allrs41556312
SNP Nexus

SNPshotrs41556312
SNPdbers41556312
MSV3drs41556312
GWAS Ctlgrs41556312
Max Magnitude0
ClinVar
Risk rs41556312(G;G)
Alt rs41556312(G;G)
Reference rs41556312(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324207A>C
CLNSRC
CLNACC