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rs41561516

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41561516(C;G)
Make rs41561516(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943951
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41561516
ebirs41561516
HLIrs41561516
Exacrs41561516
Varsomers41561516
Maprs41561516
PheGenIrs41561516
hapmaprs41561516
1000 genomesrs41561516
hgdprs41561516
ensemblrs41561516
gopubmedrs41561516
geneviewrs41561516
scholarrs41561516
googlers41561516
pharmgkbrs41561516
gwascentralrs41561516
openSNPrs41561516
23andMers41561516
23andMe allrs41561516
SNP Nexus

SNPshotrs41561516
SNPdbers41561516
MSV3drs41561516
GWAS Ctlgrs41561516
GMAF0.003214
Max Magnitude0
ClinVar
Risk rs41561516(G,T;G,T)
Alt rs41561516(G,T;G,T)
Reference rs41561516(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911728C>T
CLNSRC
CLNACC