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rs41563615

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41563615(A;A)
Make rs41563615(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356598
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41563615
ebirs41563615
HLIrs41563615
Exacrs41563615
Varsomers41563615
Maprs41563615
PheGenIrs41563615
hapmaprs41563615
1000 genomesrs41563615
hgdprs41563615
ensemblrs41563615
gopubmedrs41563615
geneviewrs41563615
scholarrs41563615
googlers41563615
pharmgkbrs41563615
gwascentralrs41563615
openSNPrs41563615
23andMers41563615
23andMe allrs41563615
SNP Nexus

SNPshotrs41563615
SNPdbers41563615
MSV3drs41563615
GWAS Ctlgrs41563615
GMAF0.05464
Max Magnitude0
ClinVar
Risk rs41563615(A;A)
Alt rs41563615(A;A)
Reference rs41563615(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324375G>T
CLNSRC
CLNACC