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rs41553518

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41553518(C;T)
Make rs41553518(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position31355813
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41553518
ebirs41553518
HLIrs41553518
Exacrs41553518
Varsomers41553518
Maprs41553518
PheGenIrs41553518
hapmaprs41553518
1000 genomesrs41553518
hgdprs41553518
ensemblrs41553518
gopubmedrs41553518
geneviewrs41553518
scholarrs41553518
googlers41553518
pharmgkbrs41553518
gwascentralrs41553518
openSNPrs41553518
23andMers41553518
23andMe allrs41553518
SNP Nexus

SNPshotrs41553518
SNPdbers41553518
MSV3drs41553518
GWAS Ctlgrs41553518
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs41553518(T;T)
Alt rs41553518(T;T)
Reference rs41553518(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323590G>A
CLNSRC
CLNACC