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rs41555113

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41555113(A;A)
Make rs41555113(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942986
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41555113
ebirs41555113
HLIrs41555113
Exacrs41555113
Varsomers41555113
Maprs41555113
PheGenIrs41555113
hapmaprs41555113
1000 genomesrs41555113
hgdprs41555113
ensemblrs41555113
gopubmedrs41555113
geneviewrs41555113
scholarrs41555113
googlers41555113
pharmgkbrs41555113
gwascentralrs41555113
openSNPrs41555113
23andMers41555113
23andMe allrs41555113
SNP Nexus

SNPshotrs41555113
SNPdbers41555113
MSV3drs41555113
GWAS Ctlgrs41555113
Max Magnitude0
ClinVar
Risk rs41555113(A,G,T;A,G,T)
Alt rs41555113(A,G,T;A,G,T)
Reference rs41555113(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910763C>A; NC_000006.11:g.29910763C>G; NC_000006.11:g.29910763C>T
CLNSRC
CLNACC