Have questions? Visit https://www.reddit.com/r/SNPedia

rs41561016

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41561016(A;A)
Make rs41561016(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354834
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41561016
ebirs41561016
HLIrs41561016
Exacrs41561016
Varsomers41561016
Maprs41561016
PheGenIrs41561016
hapmaprs41561016
1000 genomesrs41561016
hgdprs41561016
ensemblrs41561016
gopubmedrs41561016
geneviewrs41561016
scholarrs41561016
googlers41561016
pharmgkbrs41561016
gwascentralrs41561016
openSNPrs41561016
23andMers41561016
23andMe allrs41561016
SNP Nexus

SNPshotrs41561016
SNPdbers41561016
MSV3drs41561016
GWAS Ctlgrs41561016
GMAF0.03306
Max Magnitude0
ClinVar
Risk rs41561016(A;A)
Alt rs41561016(A;A)
Reference rs41561016(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322611C>T
CLNSRC
CLNACC