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rs45491502

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45491502(A;A)
Make rs45491502(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942869
GeneHLA-A
is asnp
is mentioned by
dbSNPrs45491502
ebirs45491502
HLIrs45491502
Exacrs45491502
Varsomers45491502
Maprs45491502
PheGenIrs45491502
hapmaprs45491502
1000 genomesrs45491502
hgdprs45491502
ensemblrs45491502
gopubmedrs45491502
geneviewrs45491502
scholarrs45491502
googlers45491502
pharmgkbrs45491502
gwascentralrs45491502
openSNPrs45491502
23andMers45491502
23andMe allrs45491502
SNP Nexus

SNPshotrs45491502
SNPdbers45491502
MSV3drs45491502
GWAS Ctlgrs45491502
Max Magnitude0
ClinVar
Risk rs45491502(A,G,T;A,G,T)
Alt rs45491502(A,G,T;A,G,T)
Reference rs45491502(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910646C>A; NC_000006.11:g.29910646C>G; NC_000006.11:g.29910646C>T
CLNSRC
CLNACC