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rs786204063

From SNPedia

Orientationminus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs786204063(-;-)
Make rs786204063(-;CTT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position173911959
GeneSERPINC1
is asnp
is mentioned by
dbSNPrs786204063
ebirs786204063
HLIrs786204063
Exacrs786204063
Varsomers786204063
Maprs786204063
PheGenIrs786204063
hapmaprs786204063
1000 genomesrs786204063
hgdprs786204063
ensemblrs786204063
gopubmedrs786204063
geneviewrs786204063
scholarrs786204063
googlers786204063
pharmgkbrs786204063
gwascentralrs786204063
openSNPrs786204063
23andMers786204063
23andMe allrs786204063
SNP Nexus

SNPshotrs786204063
SNPdbers786204063
MSV3drs786204063
GWAS Ctlgrs786204063
Max Magnitude0
ClinVar
Risk rs786204063(;)
Alt rs786204063(;)
Reference rs786204063(CTT;CTT)
Significance Pathogenic
Disease Antithrombin III deficiency
Variation info
Gene SERPINC1
CLNDBN Antithrombin III deficiency
Reversed 1
HGVS NC_000001.10:g.173881097_173881099delAAG
CLNSRC
CLNACC RCV000167937.2,