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rs41551615

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41551615(A;A)
Make rs41551615(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356791
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41551615
ebirs41551615
HLIrs41551615
Exacrs41551615
Varsomers41551615
Maprs41551615
PheGenIrs41551615
hapmaprs41551615
1000 genomesrs41551615
hgdprs41551615
ensemblrs41551615
gopubmedrs41551615
geneviewrs41551615
scholarrs41551615
googlers41551615
pharmgkbrs41551615
gwascentralrs41551615
openSNPrs41551615
23andMers41551615
23andMe allrs41551615
SNP Nexus

SNPshotrs41551615
SNPdbers41551615
MSV3drs41551615
GWAS Ctlgrs41551615
Max Magnitude0
ClinVar
Risk rs41551615(A,C,T;A,C,T)
Alt rs41551615(A,C,T;A,C,T)
Reference rs41551615(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324568C>A; NC_000006.11:g.31324568C>G; NC_000006.11:g.31324568C>T
CLNSRC
CLNACC