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rs41559423

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559423(A;A)
Make rs41559423(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944194
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41559423
ebirs41559423
HLIrs41559423
Exacrs41559423
Varsomers41559423
Maprs41559423
PheGenIrs41559423
hapmaprs41559423
1000 genomesrs41559423
hgdprs41559423
ensemblrs41559423
gopubmedrs41559423
geneviewrs41559423
scholarrs41559423
googlers41559423
pharmgkbrs41559423
gwascentralrs41559423
openSNPrs41559423
23andMers41559423
23andMe allrs41559423
SNP Nexus

SNPshotrs41559423
SNPdbers41559423
MSV3drs41559423
GWAS Ctlgrs41559423
Max Magnitude0
ClinVar
Risk rs41559423(A;A)
Alt rs41559423(A;A)
Reference rs41559423(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911971G>A
CLNSRC
CLNACC