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rs41558913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41558913(A;A)
Make rs41558913(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943488
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41558913
ebirs41558913
HLIrs41558913
Exacrs41558913
Varsomers41558913
Maprs41558913
PheGenIrs41558913
hapmaprs41558913
1000 genomesrs41558913
hgdprs41558913
ensemblrs41558913
gopubmedrs41558913
geneviewrs41558913
scholarrs41558913
googlers41558913
pharmgkbrs41558913
gwascentralrs41558913
openSNPrs41558913
23andMers41558913
23andMe allrs41558913
SNP Nexus

SNPshotrs41558913
SNPdbers41558913
MSV3drs41558913
GWAS Ctlgrs41558913
Max Magnitude0
ClinVar
Risk rs41558913(A,G,T;A,G,T)
Alt rs41558913(A,G,T;A,G,T)
Reference rs41558913(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911265C>A; NC_000006.11:g.29911265C>G; NC_000006.11:g.29911265C>T
CLNSRC
CLNACC