rs786204063

Orientation

minus

Stabilized

minus

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

Make rs786204063(-;-)

Make rs786204063(-;CTT)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

173911959

Gene

SERPINC1

is a	snp
is	mentioned by
dbSNP	rs786204063
dbSNP (classic)	rs786204063
ClinGen	rs786204063
ebi	rs786204063
HLI	rs786204063
Exac	rs786204063
Gnomad	rs786204063
Varsome	rs786204063
LitVar	rs786204063
Map	rs786204063
PheGenI	rs786204063
Biobank	rs786204063
1000 genomes	rs786204063
hgdp	rs786204063
ensembl	rs786204063
geneview	rs786204063
scholar	rs786204063
google	rs786204063
pharmgkb	rs786204063
gwascentral	rs786204063
openSNP	rs786204063
23andMe	rs786204063
SNPshot	rs786204063
SNPdbe	rs786204063
MSV3d	rs786204063
GWAS Ctlg	rs786204063

Max Magnitude

0

ClinVar
Risk	rs786204063(-;-)
Alt	rs786204063(-;-)
Reference	Rs786204063(CTT;CTT)
Significance	Pathogenic
Disease	Antithrombin III deficiency
Variation	info
Gene	SERPINC1
CLNDBN	Antithrombin III deficiency
Reversed	1
HGVS	NC_000001.10:g.173881097_173881099delAAG
CLNSRC
CLNACC	RCV000167937.2,