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rs41559117

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41559117(A;G)
Make rs41559117(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942883
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41559117
ebirs41559117
HLIrs41559117
Exacrs41559117
Varsomers41559117
Maprs41559117
PheGenIrs41559117
hapmaprs41559117
1000 genomesrs41559117
hgdprs41559117
ensemblrs41559117
gopubmedrs41559117
geneviewrs41559117
scholarrs41559117
googlers41559117
pharmgkbrs41559117
gwascentralrs41559117
openSNPrs41559117
23andMers41559117
23andMe allrs41559117
SNP Nexus

SNPshotrs41559117
SNPdbers41559117
MSV3drs41559117
GWAS Ctlgrs41559117
GMAF0.01653
Max Magnitude0
ClinVar
Risk rs41559117(C,G;C,G)
Alt rs41559117(C,G;C,G)
Reference rs41559117(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910660A>G
CLNSRC
CLNACC