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rs41557912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41557912(G;G)
Make rs41557912(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945424
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41557912
ebirs41557912
HLIrs41557912
Exacrs41557912
Varsomers41557912
Maprs41557912
PheGenIrs41557912
hapmaprs41557912
1000 genomesrs41557912
hgdprs41557912
ensemblrs41557912
gopubmedrs41557912
geneviewrs41557912
scholarrs41557912
googlers41557912
pharmgkbrs41557912
gwascentralrs41557912
openSNPrs41557912
23andMers41557912
23andMe allrs41557912
SNP Nexus

SNPshotrs41557912
SNPdbers41557912
MSV3drs41557912
GWAS Ctlgrs41557912
Max Magnitude0
ClinVar
Risk rs41557912(G;G)
Alt rs41557912(G;G)
Reference rs41557912(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29913201T>G
CLNSRC
CLNACC