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rs45562634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45562634(C;G)
Make rs45562634(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944152
GeneHLA-A
is asnp
is mentioned by
dbSNPrs45562634
ebirs45562634
HLIrs45562634
Exacrs45562634
Varsomers45562634
Maprs45562634
PheGenIrs45562634
hapmaprs45562634
1000 genomesrs45562634
hgdprs45562634
ensemblrs45562634
gopubmedrs45562634
geneviewrs45562634
scholarrs45562634
googlers45562634
pharmgkbrs45562634
gwascentralrs45562634
openSNPrs45562634
23andMers45562634
23andMe allrs45562634
SNP Nexus

SNPshotrs45562634
SNPdbers45562634
MSV3drs45562634
GWAS Ctlgrs45562634
Max Magnitude0
ClinVar
Risk rs45562634(G,T;G,T)
Alt rs45562634(G,T;G,T)
Reference rs45562634(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911929C>G; NC_000006.11:g.29911929C>T
CLNSRC
CLNACC