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rs764220898

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs764220898(C;G)
Make rs764220898(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position94381043
GeneSERPINA1
is asnp
is mentioned by
dbSNPrs764220898
ebirs764220898
HLIrs764220898
Exacrs764220898
Varsomers764220898
Maprs764220898
PheGenIrs764220898
hapmaprs764220898
1000 genomesrs764220898
hgdprs764220898
ensemblrs764220898
gopubmedrs764220898
geneviewrs764220898
scholarrs764220898
googlers764220898
pharmgkbrs764220898
gwascentralrs764220898
openSNPrs764220898
23andMers764220898
23andMe allrs764220898
SNP Nexus

SNPshotrs764220898
SNPdbers764220898
MSV3drs764220898
GWAS Ctlgrs764220898
Max Magnitude0
ClinVar
Risk rs764220898(G;G)
Alt rs764220898(G;G)
Reference rs764220898(C;C)
Significance Probable-Pathogenic
Disease Alpha-1-antitrypsin deficiency
Variation info
Gene SERPINA1
CLNDBN Alpha-1-antitrypsin deficiency
Reversed 0
HGVS NC_000014.8:g.94847380C>G
CLNSRC
CLNACC RCV000169405.1,