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rs121909566

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909566(A;A)
Make rs121909566(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position173904013
GeneSERPINC1
is asnp
is mentioned by
dbSNPrs121909566
ebirs121909566
HLIrs121909566
Exacrs121909566
Varsomers121909566
Maprs121909566
PheGenIrs121909566
hapmaprs121909566
1000 genomesrs121909566
hgdprs121909566
ensemblrs121909566
gopubmedrs121909566
geneviewrs121909566
scholarrs121909566
googlers121909566
pharmgkbrs121909566
gwascentralrs121909566
openSNPrs121909566
23andMers121909566
23andMe allrs121909566
SNP Nexus

SNPshotrs121909566
SNPdbers121909566
MSV3drs121909566
GWAS Ctlgrs121909566
Max Magnitude0
OMIM107300
Desc
Variant0037
Relatedalso
ClinVar
Risk rs121909566(A;A)
Alt rs121909566(A;A)
Reference rs121909566(G;G)
Significance Pathogenic
Disease Antithrombin III deficiency
Variation info
Gene SERPINC1
CLNDBN Antithrombin III deficiency
Reversed 1
HGVS NC_000001.10:g.173873151C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019649.27,