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rs41556816

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41556816(A;A)
Make rs41556816(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356842
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556816
ebirs41556816
HLIrs41556816
Exacrs41556816
Varsomers41556816
Maprs41556816
PheGenIrs41556816
hapmaprs41556816
1000 genomesrs41556816
hgdprs41556816
ensemblrs41556816
gopubmedrs41556816
geneviewrs41556816
scholarrs41556816
googlers41556816
pharmgkbrs41556816
gwascentralrs41556816
openSNPrs41556816
23andMers41556816
23andMe allrs41556816
SNP Nexus

SNPshotrs41556816
SNPdbers41556816
MSV3drs41556816
GWAS Ctlgrs41556816
Max Magnitude0
ClinVar
Risk rs41556816(A,T;A,T)
Alt rs41556816(A,T;A,T)
Reference rs41556816(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324619G>A; NC_000006.11:g.31324619G>T
CLNSRC
CLNACC