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rs41561215

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41561215(A;A)
Make rs41561215(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356355
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41561215
ebirs41561215
HLIrs41561215
Exacrs41561215
Varsomers41561215
Maprs41561215
PheGenIrs41561215
hapmaprs41561215
1000 genomesrs41561215
hgdprs41561215
ensemblrs41561215
gopubmedrs41561215
geneviewrs41561215
scholarrs41561215
googlers41561215
pharmgkbrs41561215
gwascentralrs41561215
openSNPrs41561215
23andMers41561215
23andMe allrs41561215
SNP Nexus

SNPshotrs41561215
SNPdbers41561215
MSV3drs41561215
GWAS Ctlgrs41561215
Max Magnitude0
ClinVar
Risk rs41561215(A,T;A,T)
Alt rs41561215(A,T;A,T)
Reference rs41561215(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324132C>A; NC_000006.11:g.31324132C>T
CLNSRC
CLNACC