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rs41562818

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41562818(A;G)
Make rs41562818(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356370
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562818
ebirs41562818
HLIrs41562818
Exacrs41562818
Varsomers41562818
Maprs41562818
PheGenIrs41562818
hapmaprs41562818
1000 genomesrs41562818
hgdprs41562818
ensemblrs41562818
gopubmedrs41562818
geneviewrs41562818
scholarrs41562818
googlers41562818
pharmgkbrs41562818
gwascentralrs41562818
openSNPrs41562818
23andMers41562818
23andMe allrs41562818
SNP Nexus

SNPshotrs41562818
SNPdbers41562818
MSV3drs41562818
GWAS Ctlgrs41562818
Max Magnitude0
ClinVar
Risk rs41562818(G;G)
Alt rs41562818(G;G)
Reference rs41562818(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324147T>C
CLNSRC
CLNACC