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rs542881762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs542881762(C;T)
Make rs542881762(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position173907528
GeneSERPINC1
is asnp
is mentioned by
dbSNPrs542881762
dbSNP (classic)rs542881762
ClinGenrs542881762
ebirs542881762
HLIrs542881762
Exacrs542881762
Gnomadrs542881762
Varsomers542881762
LitVarrs542881762
Maprs542881762
PheGenIrs542881762
Biobankrs542881762
1000 genomesrs542881762
hgdprs542881762
ensemblrs542881762
geneviewrs542881762
scholarrs542881762
googlers542881762
pharmgkbrs542881762
gwascentralrs542881762
openSNPrs542881762
23andMers542881762
23andMe allrs542881762
SNPshotrs542881762
SNPdbers542881762
MSV3drs542881762
GWAS Ctlgrs542881762
Max Magnitude0
ClinVar
Risk rs542881762(G;G) rs542881762(T;T)
Alt rs542881762(G;G) rs542881762(T;T)
Reference Rs542881762(C;C)
Significance Probable-Pathogenic
Disease Antithrombin III deficiency
Variation info
Gene SERPINC1
CLNDBN Antithrombin III deficiency
Reversed 0
HGVS NC_000001.10:g.173876666C>T
CLNSRC
CLNACC RCV000456535.1,