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rs41562913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41562913(A;A)
Make rs41562913(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356421
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562913
ebirs41562913
HLIrs41562913
Exacrs41562913
Varsomers41562913
Maprs41562913
PheGenIrs41562913
hapmaprs41562913
1000 genomesrs41562913
hgdprs41562913
ensemblrs41562913
gopubmedrs41562913
geneviewrs41562913
scholarrs41562913
googlers41562913
pharmgkbrs41562913
gwascentralrs41562913
openSNPrs41562913
23andMers41562913
23andMe allrs41562913
SNP Nexus

SNPshotrs41562913
SNPdbers41562913
MSV3drs41562913
GWAS Ctlgrs41562913
Max Magnitude0
ClinVar
Risk rs41562913(A,C,G;A,C,G)
Alt rs41562913(A,C,G;A,C,G)
Reference rs41562913(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324198A>C; NC_000006.11:g.31324198A>G; NC_000006.11:g.31324198A>T
CLNSRC
CLNACC