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rs41559912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559912(A;A)
Make rs41559912(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943020
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41559912
ebirs41559912
HLIrs41559912
Exacrs41559912
Varsomers41559912
Maprs41559912
PheGenIrs41559912
hapmaprs41559912
1000 genomesrs41559912
hgdprs41559912
ensemblrs41559912
gopubmedrs41559912
geneviewrs41559912
scholarrs41559912
googlers41559912
pharmgkbrs41559912
gwascentralrs41559912
openSNPrs41559912
23andMers41559912
23andMe allrs41559912
SNP Nexus

SNPshotrs41559912
SNPdbers41559912
MSV3drs41559912
GWAS Ctlgrs41559912
Max Magnitude0
ClinVar
Risk rs41559912(A,C,T;A,C,T)
Alt rs41559912(A,C,T;A,C,T)
Reference rs41559912(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910797G>A; NC_000006.11:g.29910797G>C; NC_000006.11:g.29910797G>T
CLNSRC
CLNACC