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rs41551316

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41551316(C;T)
Make rs41551316(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354801
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41551316
ebirs41551316
HLIrs41551316
Exacrs41551316
Varsomers41551316
Maprs41551316
PheGenIrs41551316
hapmaprs41551316
1000 genomesrs41551316
hgdprs41551316
ensemblrs41551316
gopubmedrs41551316
geneviewrs41551316
scholarrs41551316
googlers41551316
pharmgkbrs41551316
gwascentralrs41551316
openSNPrs41551316
23andMers41551316
23andMe allrs41551316
SNP Nexus

SNPshotrs41551316
SNPdbers41551316
MSV3drs41551316
GWAS Ctlgrs41551316
Max Magnitude0
ClinVar
Risk rs41551316(T;T)
Alt rs41551316(T;T)
Reference rs41551316(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322578G>A
CLNSRC
CLNACC