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rs41559615

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41559615(A;A)
Make rs41559615(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943422
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41559615
ebirs41559615
HLIrs41559615
Exacrs41559615
Varsomers41559615
Maprs41559615
PheGenIrs41559615
hapmaprs41559615
1000 genomesrs41559615
hgdprs41559615
ensemblrs41559615
gopubmedrs41559615
geneviewrs41559615
scholarrs41559615
googlers41559615
pharmgkbrs41559615
gwascentralrs41559615
openSNPrs41559615
23andMers41559615
23andMe allrs41559615
SNP Nexus

SNPshotrs41559615
SNPdbers41559615
MSV3drs41559615
GWAS Ctlgrs41559615
Max Magnitude0
ClinVar
Risk rs41559615(A,T;A,T)
Alt rs41559615(A,T;A,T)
Reference rs41559615(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911199C>A; NC_000006.11:g.29911199C>T
CLNSRC
CLNACC