rs121909570

Orientation

minus

Stabilized

minus

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

Make rs121909570(A;C)

Make rs121909570(C;C)

Reference

GRCh38 38.1/141

Chromosome

1

Position

173911923

Gene

SERPINC1

is a	snp
is	mentioned by
dbSNP	rs121909570
dbSNP (classic)	rs121909570
ClinGen	rs121909570
ebi	rs121909570
HLI	rs121909570
Exac	rs121909570
Gnomad	rs121909570
Varsome	rs121909570
LitVar	rs121909570
Map	rs121909570
PheGenI	rs121909570
Biobank	rs121909570
1000 genomes	rs121909570
hgdp	rs121909570
ensembl	rs121909570
geneview	rs121909570
scholar	rs121909570
google	rs121909570
pharmgkb	rs121909570
gwascentral	rs121909570
openSNP	rs121909570
23andMe	rs121909570
SNPshot	rs121909570
SNPdbe	rs121909570
MSV3d	rs121909570
GWAS Ctlg	rs121909570

Max Magnitude

0

OMIM	107300
Desc
Variant	0045
Related	also

ClinVar
Risk	rs121909570(C;C)
Alt	rs121909570(C;C)
Reference	Rs121909570(A;A)
Significance	Pathogenic
Disease	Antithrombin III deficiency
Variation	info
Gene	SERPINC1
CLNDBN	Antithrombin III deficiency
Reversed	1
HGVS	NC_000001.10:g.173881061T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019657.27,