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rs45617033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45617033(C;T)
Make rs45617033(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942800
GeneHLA-A
is asnp
is mentioned by
dbSNPrs45617033
ebirs45617033
HLIrs45617033
Exacrs45617033
Varsomers45617033
Maprs45617033
PheGenIrs45617033
hapmaprs45617033
1000 genomesrs45617033
hgdprs45617033
ensemblrs45617033
gopubmedrs45617033
geneviewrs45617033
scholarrs45617033
googlers45617033
pharmgkbrs45617033
gwascentralrs45617033
openSNPrs45617033
23andMers45617033
23andMe allrs45617033
SNP Nexus

SNPshotrs45617033
SNPdbers45617033
MSV3drs45617033
GWAS Ctlgrs45617033
GMAF0.02938
Max Magnitude0
ClinVar
Risk rs45617033(G,T;G,T)
Alt rs45617033(G,T;G,T)
Reference rs45617033(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910577C>G; NC_000006.11:g.29910577C>T
CLNSRC
CLNACC