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rs121909556

From SNPedia

Merged intors121909549
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909556(A;A)
Make rs121909556(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position173904010
GeneSERPINC1
is asnp
is mentioned by
dbSNPrs121909556
ebirs121909556
HLIrs121909556
Exacrs121909556
Varsomers121909556
Maprs121909556
PheGenIrs121909556
hapmaprs121909556
1000 genomesrs121909556
hgdprs121909556
ensemblrs121909556
gopubmedrs121909556
geneviewrs121909556
scholarrs121909556
googlers121909556
pharmgkbrs121909556
gwascentralrs121909556
openSNPrs121909556
23andMers121909556
23andMe allrs121909556
SNP Nexus

SNPshotrs121909556
SNPdbers121909556
MSV3drs121909556
GWAS Ctlgrs121909556
StatusMerged into rs121909549
Max Magnitude0
OMIM107300
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121909556(A;A)
Alt rs121909556(A;A)
Reference rs121909556(G;G)
Significance Pathogenic
Disease Antithrombin III deficiency
Variation info
Gene SERPINC1
CLNDBN Antithrombin III deficiency
Reversed 1
HGVS NC_000001.10:g.173873148C>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000039933.1,