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rs121909553

From SNPedia

Merged intors121909547
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909553(A;A)
Make rs121909553(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position173914726
GeneSERPINC1
is asnp
is mentioned by
dbSNPrs121909553
ebirs121909553
HLIrs121909553
Exacrs121909553
Varsomers121909553
Maprs121909553
PheGenIrs121909553
hapmaprs121909553
1000 genomesrs121909553
hgdprs121909553
ensemblrs121909553
gopubmedrs121909553
geneviewrs121909553
scholarrs121909553
googlers121909553
pharmgkbrs121909553
gwascentralrs121909553
openSNPrs121909553
23andMers121909553
23andMe allrs121909553
SNP Nexus

SNPshotrs121909553
SNPdbers121909553
MSV3drs121909553
GWAS Ctlgrs121909553
StatusMerged into rs121909547
Max Magnitude0
OMIM107300
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121909553(A;A)
Alt rs121909553(A;A)
Reference rs121909553(C;C)
Significance Pathogenic
Disease Antithrombin III deficiency
Variation info
Gene SERPINC1
CLNDBN Antithrombin III deficiency
Reversed 1
HGVS NC_000001.10:g.173883864G>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000039929.1,