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rs41553212

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(C;C) 0 common in clinvar
Make rs41553212(A;T)
Make rs41553212(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943733
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41553212
ebirs41553212
HLIrs41553212
Exacrs41553212
Varsomers41553212
Maprs41553212
PheGenIrs41553212
hapmaprs41553212
1000 genomesrs41553212
hgdprs41553212
ensemblrs41553212
gopubmedrs41553212
geneviewrs41553212
scholarrs41553212
googlers41553212
pharmgkbrs41553212
gwascentralrs41553212
openSNPrs41553212
23andMers41553212
23andMe allrs41553212
SNP Nexus

SNPshotrs41553212
SNPdbers41553212
MSV3drs41553212
GWAS Ctlgrs41553212
GMAF0.02663
Max Magnitude0
ClinVar
Risk rs41553212(T;T)
Alt rs41553212(T;T)
Reference rs41553212(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911510A>T
CLNSRC
CLNACC