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rs45482492

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45482492(A;A)
Make rs45482492(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943378
GeneHLA-A
is asnp
is mentioned by
dbSNPrs45482492
ebirs45482492
HLIrs45482492
Exacrs45482492
Varsomers45482492
Maprs45482492
PheGenIrs45482492
hapmaprs45482492
1000 genomesrs45482492
hgdprs45482492
ensemblrs45482492
gopubmedrs45482492
geneviewrs45482492
scholarrs45482492
googlers45482492
pharmgkbrs45482492
gwascentralrs45482492
openSNPrs45482492
23andMers45482492
23andMe allrs45482492
SNP Nexus

SNPshotrs45482492
SNPdbers45482492
MSV3drs45482492
GWAS Ctlgrs45482492
Max Magnitude0
ClinVar
Risk rs45482492(A,C,T;A,C,T)
Alt rs45482492(A,C,T;A,C,T)
Reference rs45482492(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911155G>A; NC_000006.11:g.29911155G>C; NC_000006.11:g.29911155G>T
CLNSRC
CLNACC