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rs45604832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45604832(C;T)
Make rs45604832(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943068
GeneHLA-A
is asnp
is mentioned by
dbSNPrs45604832
ebirs45604832
HLIrs45604832
Exacrs45604832
Varsomers45604832
Maprs45604832
PheGenIrs45604832
hapmaprs45604832
1000 genomesrs45604832
hgdprs45604832
ensemblrs45604832
gopubmedrs45604832
geneviewrs45604832
scholarrs45604832
googlers45604832
pharmgkbrs45604832
gwascentralrs45604832
openSNPrs45604832
23andMers45604832
23andMe allrs45604832
SNP Nexus

SNPshotrs45604832
SNPdbers45604832
MSV3drs45604832
GWAS Ctlgrs45604832
Max Magnitude0
ClinVar
Risk rs45604832(T;T)
Alt rs45604832(T;T)
Reference rs45604832(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910845C>T
CLNSRC
CLNACC