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rs1802959

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1802959(A;A)
Make rs1802959(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position94378628
GeneSERPINA1
is asnp
is mentioned by
dbSNPrs1802959
ebirs1802959
HLIrs1802959
Exacrs1802959
Varsomers1802959
Maprs1802959
PheGenIrs1802959
hapmaprs1802959
1000 genomesrs1802959
hgdprs1802959
ensemblrs1802959
gopubmedrs1802959
geneviewrs1802959
scholarrs1802959
googlers1802959
pharmgkbrs1802959
gwascentralrs1802959
openSNPrs1802959
23andMers1802959
23andMe allrs1802959
SNP Nexus

SNPshotrs1802959
SNPdbers1802959
MSV3drs1802959
GWAS Ctlgrs1802959
Merged fromRs28929475
Max Magnitude0
OMIM107400
Desc
Variant0029
Relatedalso


ClinVar
Risk rs1802959(A,C;A,C)
Alt rs1802959(A,C;A,C)
Reference rs1802959(G;G)
Significance Other
Disease PI W(BETHESDA)
Variation info
Gene SERPINA1
CLNDBN PI W(BETHESDA)
Reversed 1
HGVS NC_000014.8:g.94844965C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019596.3,



[PMID 2185272OA-icon.png] Alpha 1-antitrypsin deficiency, emphysema, and liver disease. Genetic basis and strategies for therapy.

[PMID 2240842] Molecular analysis of the heterogeneity among the P-family of alpha-1-antitrypsin alleles.