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rs121912712

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912712(A;A)
Make rs121912712(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position94378547
GeneSERPINA1
is asnp
is mentioned by
dbSNPrs121912712
ebirs121912712
HLIrs121912712
Exacrs121912712
Varsomers121912712
Maprs121912712
PheGenIrs121912712
hapmaprs121912712
1000 genomesrs121912712
hgdprs121912712
ensemblrs121912712
gopubmedrs121912712
geneviewrs121912712
scholarrs121912712
googlers121912712
pharmgkbrs121912712
gwascentralrs121912712
openSNPrs121912712
23andMers121912712
23andMe allrs121912712
SNP Nexus

SNPshotrs121912712
SNPdbers121912712
MSV3drs121912712
GWAS Ctlgrs121912712
GMAF0.0004591
Max Magnitude0
OMIM107400
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121912712(A;A)
Alt rs121912712(A;A)
Reference rs121912712(G;G)
Significance Other
Disease PI CHRISTCHURCH
Variation info
Gene SERPINA1
CLNDBN PI CHRISTCHURCH
Reversed 1
HGVS NC_000014.8:g.94844884C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019564.3,