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rs41552627

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41552627(C;T)
Make rs41552627(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943203
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41552627
ebirs41552627
HLIrs41552627
Exacrs41552627
Varsomers41552627
Maprs41552627
PheGenIrs41552627
hapmaprs41552627
1000 genomesrs41552627
hgdprs41552627
ensemblrs41552627
gopubmedrs41552627
geneviewrs41552627
scholarrs41552627
googlers41552627
pharmgkbrs41552627
gwascentralrs41552627
openSNPrs41552627
23andMers41552627
23andMe allrs41552627
SNP Nexus

SNPshotrs41552627
SNPdbers41552627
MSV3drs41552627
GWAS Ctlgrs41552627
GMAF0.06336
Max Magnitude0
ClinVar
Risk rs41552627(T;T)
Alt rs41552627(T;T)
Reference rs41552627(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910980C>T
CLNSRC
CLNACC