rs121909548

Orientation

minus

Stabilized

minus

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

Make rs121909548(C;C)

Make rs121909548(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

173904038

Gene

SERPINC1

is a	snp
is	mentioned by
dbSNP	rs121909548
dbSNP (classic)	rs121909548
ClinGen	rs121909548
ebi	rs121909548
HLI	rs121909548
Exac	rs121909548
Gnomad	rs121909548
Varsome	rs121909548
LitVar	rs121909548
Map	rs121909548
PheGenI	rs121909548
Biobank	rs121909548
1000 genomes	rs121909548
hgdp	rs121909548
ensembl	rs121909548
geneview	rs121909548
scholar	rs121909548
google	rs121909548
pharmgkb	rs121909548
gwascentral	rs121909548
openSNP	rs121909548
23andMe	rs121909548
SNPshot	rs121909548
SNPdbe	rs121909548
MSV3d	rs121909548
GWAS Ctlg	rs121909548

Merged from

Rs121909559, Rs28930978

GMAF

0.0004591

Max Magnitude

0

OMIM	107300
Desc
Variant	0007
Related	also

OMIM	107300
Desc
Variant	0027
Related	also

ClinVar
Risk	rs121909548(C;C) rs121909548(T;T)
Alt	rs121909548(C;C) rs121909548(T;T)
Reference	Rs121909548(G;G)
Significance	Other
Disease	Antithrombin III deficiency Antithrombin deficiency not specified
Variation	info
Gene	SERPINC1
CLNDBN	Antithrombin III deficiency Antithrombin deficiency not specified
Reversed	1
HGVS	NC_000001.10:g.173873176C>A; NC_000001.10:g.173873176C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019639.27, RCV000148884.1, RCV000249153.1, RCV000019623.28,