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rs20546

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs20546(C;T)
Make rs20546(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position94382814
GeneSERPINA1
is asnp
is mentioned by
dbSNPrs20546
ebirs20546
HLIrs20546
Exacrs20546
Varsomers20546
Maprs20546
PheGenIrs20546
hapmaprs20546
1000 genomesrs20546
hgdprs20546
ensemblrs20546
gopubmedrs20546
geneviewrs20546
scholarrs20546
googlers20546
pharmgkbrs20546
gwascentralrs20546
openSNPrs20546
23andMers20546
23andMe allrs20546
SNP Nexus

SNPshotrs20546
SNPdbers20546
MSV3drs20546
GWAS Ctlgrs20546
Max Magnitude0
? (C;C) (C;T) (T;T) 28


ClinVar
Risk rs20546(T;T)
Alt rs20546(T;T)
Reference rs20546(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene SERPINA1
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.94849151G>A
CLNSRC
CLNACC RCV000155575.1,