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rs121909569

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909569(C;C)
Make rs121909569(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position173911981
GeneSERPINC1
is asnp
is mentioned by
dbSNPrs121909569
ebirs121909569
HLIrs121909569
Exacrs121909569
Varsomers121909569
Maprs121909569
PheGenIrs121909569
hapmaprs121909569
1000 genomesrs121909569
hgdprs121909569
ensemblrs121909569
gopubmedrs121909569
geneviewrs121909569
scholarrs121909569
googlers121909569
pharmgkbrs121909569
gwascentralrs121909569
openSNPrs121909569
23andMers121909569
23andMe allrs121909569
SNP Nexus

SNPshotrs121909569
SNPdbers121909569
MSV3drs121909569
GWAS Ctlgrs121909569
Max Magnitude0
OMIM107300
Desc
Variant0043
Relatedalso
ClinVar
Risk rs121909569(C;C)
Alt rs121909569(C;C)
Reference rs121909569(T;T)
Significance Pathogenic
Disease Antithrombin III deficiency
Variation info
Gene SERPINC1
CLNDBN Antithrombin III deficiency
Reversed 1
HGVS NC_000001.10:g.173881119A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019655.23,