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rs863224495

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224495(-;-)
Make rs863224495(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position173909645
GeneSERPINC1
is asnp
is mentioned by
dbSNPrs863224495
dbSNP (classic)rs863224495
ClinGenrs863224495
ebirs863224495
HLIrs863224495
Exacrs863224495
Gnomadrs863224495
Varsomers863224495
LitVarrs863224495
Maprs863224495
PheGenIrs863224495
Biobankrs863224495
1000 genomesrs863224495
hgdprs863224495
ensemblrs863224495
geneviewrs863224495
scholarrs863224495
googlers863224495
pharmgkbrs863224495
gwascentralrs863224495
openSNPrs863224495
23andMers863224495
SNPshotrs863224495
SNPdbers863224495
MSV3drs863224495
GWAS Ctlgrs863224495
Max Magnitude0
ClinVar
Risk rs863224495(-;-)
Alt rs863224495(-;-)
Reference Rs863224495(C;C)
Significance Pathogenic
Disease Antithrombin III deficiency
Variation info
Gene SERPINC1
CLNDBN Antithrombin III deficiency
Reversed 1
HGVS NC_000001.10:g.173878783delG
CLNSRC
CLNACC RCV000197842.2,