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rs41556913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41556913(C;T)
Make rs41556913(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943275
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41556913
ebirs41556913
HLIrs41556913
Exacrs41556913
Varsomers41556913
Maprs41556913
PheGenIrs41556913
hapmaprs41556913
1000 genomesrs41556913
hgdprs41556913
ensemblrs41556913
gopubmedrs41556913
geneviewrs41556913
scholarrs41556913
googlers41556913
pharmgkbrs41556913
gwascentralrs41556913
openSNPrs41556913
23andMers41556913
23andMe allrs41556913
SNP Nexus

SNPshotrs41556913
SNPdbers41556913
MSV3drs41556913
GWAS Ctlgrs41556913
Max Magnitude0
ClinVar
Risk rs41556913(T;T)
Alt rs41556913(T;T)
Reference rs41556913(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911052C>T
CLNSRC
CLNACC