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rs41552715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552715(A;A)
Make rs41552715(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356711
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552715
ebirs41552715
HLIrs41552715
Exacrs41552715
Varsomers41552715
Maprs41552715
PheGenIrs41552715
hapmaprs41552715
1000 genomesrs41552715
hgdprs41552715
ensemblrs41552715
gopubmedrs41552715
geneviewrs41552715
scholarrs41552715
googlers41552715
pharmgkbrs41552715
gwascentralrs41552715
openSNPrs41552715
23andMers41552715
23andMe allrs41552715
SNP Nexus

SNPshotrs41552715
SNPdbers41552715
MSV3drs41552715
GWAS Ctlgrs41552715
Max Magnitude0
ClinVar
Risk rs41552715(A,C,T;A,C,T)
Alt rs41552715(A,C,T;A,C,T)
Reference rs41552715(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324488C>A; NC_000006.11:g.31324488C>G; NC_000006.11:g.31324488C>T
CLNSRC
CLNACC