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rs41562813

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41562813(-;-)
Make rs41562813(-;A)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324030
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562813
ebirs41562813
HLIrs41562813
Exacrs41562813
Varsomers41562813
Maprs41562813
PheGenIrs41562813
hapmaprs41562813
1000 genomesrs41562813
hgdprs41562813
ensemblrs41562813
gopubmedrs41562813
geneviewrs41562813
scholarrs41562813
googlers41562813
pharmgkbrs41562813
gwascentralrs41562813
openSNPrs41562813
23andMers41562813
23andMe allrs41562813
SNP Nexus

SNPshotrs41562813
SNPdbers41562813
MSV3drs41562813
GWAS Ctlgrs41562813
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41562813(;)
Alt rs41562813(;)
Reference rs41562813(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324030delT
CLNSRC
CLNACC