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rs41562812

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41562812(C;T)
Make rs41562812(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356947
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562812
ebirs41562812
HLIrs41562812
Exacrs41562812
Varsomers41562812
Maprs41562812
PheGenIrs41562812
hapmaprs41562812
1000 genomesrs41562812
hgdprs41562812
ensemblrs41562812
gopubmedrs41562812
geneviewrs41562812
scholarrs41562812
googlers41562812
pharmgkbrs41562812
gwascentralrs41562812
openSNPrs41562812
23andMers41562812
23andMe allrs41562812
SNP Nexus

SNPshotrs41562812
SNPdbers41562812
MSV3drs41562812
GWAS Ctlgrs41562812
Max Magnitude0
ClinVar
Risk rs41562812(T;T)
Alt rs41562812(T;T)
Reference rs41562812(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324724G>A
CLNSRC
CLNACC