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rs41563315

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41563315(A;A)
Make rs41563315(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356834
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41563315
ebirs41563315
HLIrs41563315
Exacrs41563315
Varsomers41563315
Maprs41563315
PheGenIrs41563315
hapmaprs41563315
1000 genomesrs41563315
hgdprs41563315
ensemblrs41563315
gopubmedrs41563315
geneviewrs41563315
scholarrs41563315
googlers41563315
pharmgkbrs41563315
gwascentralrs41563315
openSNPrs41563315
23andMers41563315
23andMe allrs41563315
SNP Nexus

SNPshotrs41563315
SNPdbers41563315
MSV3drs41563315
GWAS Ctlgrs41563315
Max Magnitude0
ClinVar
Risk rs41563315(A,C,T;A,C,T)
Alt rs41563315(A,C,T;A,C,T)
Reference rs41563315(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324611C>A; NC_000006.11:g.31324611C>G; NC_000006.11:g.31324611C>T
CLNSRC
CLNACC