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rs41552712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552712(C;C)
Make rs41552712(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943487
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41552712
ebirs41552712
HLIrs41552712
Exacrs41552712
Varsomers41552712
Maprs41552712
PheGenIrs41552712
hapmaprs41552712
1000 genomesrs41552712
hgdprs41552712
ensemblrs41552712
gopubmedrs41552712
geneviewrs41552712
scholarrs41552712
googlers41552712
pharmgkbrs41552712
gwascentralrs41552712
openSNPrs41552712
23andMers41552712
23andMe allrs41552712
SNP Nexus

SNPshotrs41552712
SNPdbers41552712
MSV3drs41552712
GWAS Ctlgrs41552712
Max Magnitude0
ClinVar
Risk rs41552712(C,T;C,T)
Alt rs41552712(C,T;C,T)
Reference rs41552712(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911264G>C; NC_000006.11:g.29911264G>T
CLNSRC
CLNACC