rs121909565

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs121909565(C;C)

Make rs121909565(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

173909564

Gene

SERPINC1

is a	snp
is	mentioned by
dbSNP	rs121909565
dbSNP (classic)	rs121909565
ClinGen	rs121909565
ebi	rs121909565
HLI	rs121909565
Exac	rs121909565
Gnomad	rs121909565
Varsome	rs121909565
LitVar	rs121909565
Map	rs121909565
PheGenI	rs121909565
Biobank	rs121909565
1000 genomes	rs121909565
hgdp	rs121909565
ensembl	rs121909565
geneview	rs121909565
scholar	rs121909565
google	rs121909565
pharmgkb	rs121909565
gwascentral	rs121909565
openSNP	rs121909565
23andMe	rs121909565
SNPshot	rs121909565
SNPdbe	rs121909565
MSV3d	rs121909565
GWAS Ctlg	rs121909565

Max Magnitude

0

OMIM	107300
Desc
Variant	0036
Related	also

ClinVar
Risk	rs121909565(C;C)
Alt	rs121909565(C;C)
Reference	Rs121909565(T;T)
Significance	Pathogenic
Disease	Antithrombin III deficiency
Variation	info
Gene	SERPINC1
CLNDBN	Antithrombin III deficiency
Reversed	1
HGVS	NC_000001.10:g.173878702A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019648.23,