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rs41559716

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41559716(A;G)
Make rs41559716(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942916
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41559716
ebirs41559716
HLIrs41559716
Exacrs41559716
Varsomers41559716
Maprs41559716
PheGenIrs41559716
hapmaprs41559716
1000 genomesrs41559716
hgdprs41559716
ensemblrs41559716
gopubmedrs41559716
geneviewrs41559716
scholarrs41559716
googlers41559716
pharmgkbrs41559716
gwascentralrs41559716
openSNPrs41559716
23andMers41559716
23andMe allrs41559716
SNP Nexus

SNPshotrs41559716
SNPdbers41559716
MSV3drs41559716
GWAS Ctlgrs41559716
Max Magnitude0
ClinVar
Risk rs41559716(G;G)
Alt rs41559716(G;G)
Reference rs41559716(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910693A>G
CLNSRC
CLNACC