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rs41562914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41562914(A;C)
Make rs41562914(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356825
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562914
ebirs41562914
HLIrs41562914
Exacrs41562914
Varsomers41562914
Maprs41562914
PheGenIrs41562914
hapmaprs41562914
1000 genomesrs41562914
hgdprs41562914
ensemblrs41562914
gopubmedrs41562914
geneviewrs41562914
scholarrs41562914
googlers41562914
pharmgkbrs41562914
gwascentralrs41562914
openSNPrs41562914
23andMers41562914
23andMe allrs41562914
SNP Nexus

SNPshotrs41562914
SNPdbers41562914
MSV3drs41562914
GWAS Ctlgrs41562914
Max Magnitude0
ClinVar
Risk rs41562914(C,G,T;C,G,T)
Alt rs41562914(C,G,T;C,G,T)
Reference rs41562914(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324602T>A; NC_000006.11:g.31324602T>C; NC_000006.11:g.31324602T>G
CLNSRC
CLNACC