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rs41272547

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41272547(A;A)
Make rs41272547(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942280
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41272547
ebirs41272547
HLIrs41272547
Exacrs41272547
Varsomers41272547
Maprs41272547
PheGenIrs41272547
hapmaprs41272547
1000 genomesrs41272547
hgdprs41272547
ensemblrs41272547
gopubmedrs41272547
geneviewrs41272547
scholarrs41272547
googlers41272547
pharmgkbrs41272547
gwascentralrs41272547
openSNPrs41272547
23andMers41272547
23andMe allrs41272547
SNP Nexus

SNPshotrs41272547
SNPdbers41272547
MSV3drs41272547
GWAS Ctlgrs41272547
GMAF0.07392
Max Magnitude0
ClinVar
Risk rs41272547(A;A)
Alt rs41272547(A;A)
Reference rs41272547(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910057C>A
CLNSRC
CLNACC