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rs17473

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17473(C;G)
Make rs17473(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position94619305
GeneSERPINA3
is asnp
is mentioned by
dbSNPrs17473
ebirs17473
HLIrs17473
Exacrs17473
Varsomers17473
Maprs17473
PheGenIrs17473
hapmaprs17473
1000 genomesrs17473
hgdprs17473
ensemblrs17473
gopubmedrs17473
geneviewrs17473
scholarrs17473
googlers17473
pharmgkbrs17473
gwascentralrs17473
openSNPrs17473
23andMers17473
23andMe allrs17473
SNP Nexus

SNPshotrs17473
SNPdbers17473
MSV3drs17473
GWAS Ctlgrs17473
GMAF0.001837
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 21067581OA-icon.png] finds no association between rs17473 and pulmonary emphysema
OMIM107280
Desc
Variant0004
Relatedalso


ClinVar
Risk rs17473(G,T;G,T)
Alt rs17473(G,T;G,T)
Reference rs17473(C;C)
Significance Pathogenic
Disease ANTICHYMOTRYPSIN BONN 1
Variation info
Gene SERPINA3
CLNDBN ANTICHYMOTRYPSIN BONN 1
Reversed 0
HGVS NC_000014.8:g.95085642C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019666.27,



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