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rs1800463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1800463(C;C)
Make rs1800463(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position94614674
GeneSERPINA3
is asnp
is mentioned by
dbSNPrs1800463
ebirs1800463
HLIrs1800463
Exacrs1800463
Varsomers1800463
Maprs1800463
PheGenIrs1800463
hapmaprs1800463
1000 genomesrs1800463
hgdprs1800463
ensemblrs1800463
gopubmedrs1800463
geneviewrs1800463
scholarrs1800463
googlers1800463
pharmgkbrs1800463
gwascentralrs1800463
openSNPrs1800463
23andMers1800463
23andMe allrs1800463
SNP Nexus

SNPshotrs1800463
SNPdbers1800463
MSV3drs1800463
GWAS Ctlgrs1800463
Max Magnitude0
[PMID 21067581OA-icon.png] finds no association between rs1800463 and pulmonary emphysema
OMIM107280
Desc
Variant0003
Relatedalso
ClinVar
Risk rs1800463(C;C)
Alt rs1800463(C;C)
Reference rs1800463(T;T)
Significance Pathogenic
Disease ANTICHYMOTRYPSIN BOCHUM 1
Variation info
Gene SERPINA3
CLNDBN ANTICHYMOTRYPSIN BOCHUM 1
Reversed 0
HGVS NC_000014.8:g.95081011T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019665.27,


[PMID 17054776OA-icon.png] The genetics of chronic obstructive pulmonary disease.