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rs41559412

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559412(C;C)
Make rs41559412(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943040
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41559412
ebirs41559412
HLIrs41559412
Exacrs41559412
Varsomers41559412
Maprs41559412
PheGenIrs41559412
hapmaprs41559412
1000 genomesrs41559412
hgdprs41559412
ensemblrs41559412
gopubmedrs41559412
geneviewrs41559412
scholarrs41559412
googlers41559412
pharmgkbrs41559412
gwascentralrs41559412
openSNPrs41559412
23andMers41559412
23andMe allrs41559412
SNP Nexus

SNPshotrs41559412
SNPdbers41559412
MSV3drs41559412
GWAS Ctlgrs41559412
GMAF0.02801
Max Magnitude0
ClinVar
Risk rs41559412(C;C)
Alt rs41559412(C;C)
Reference rs41559412(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910817G>C
CLNSRC
CLNACC