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rs45572937

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs45572937(C;C)
Make rs45572937(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943008
GeneHLA-A
is asnp
is mentioned by
dbSNPrs45572937
dbSNP (old)rs45572937
ClinGenrs45572937
ebirs45572937
HLIrs45572937
Exacrs45572937
Varsomers45572937
Maprs45572937
PheGenIrs45572937
Biobankrs45572937
1000 genomesrs45572937
hgdprs45572937
ensemblrs45572937
gopubmedrs45572937
geneviewrs45572937
scholarrs45572937
googlers45572937
pharmgkbrs45572937
gwascentralrs45572937
openSNPrs45572937
23andMers45572937
23andMe allrs45572937
SNP Nexus

SNPshotrs45572937
SNPdbers45572937
MSV3drs45572937
GWAS Ctlgrs45572937
Max Magnitude0
ClinVar
Risk rs45572937(C;C)
Alt rs45572937(C;C)
Reference Rs45572937(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910785T>C
CLNSRC
CLNACC