rs863224838

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(GG;T)	5	Partial protein-S deficiency; higher risk for blood clotting related issues
(T;T)	0	common in clinvar

Make rs863224838(GG;GG)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

93893121

Gene

PROS1

is a	snp
is	mentioned by
dbSNP	rs863224838
dbSNP (classic)	rs863224838
ClinGen	rs863224838
ebi	rs863224838
HLI	rs863224838
Exac	rs863224838
Gnomad	rs863224838
Varsome	rs863224838
LitVar	rs863224838
Map	rs863224838
PheGenI	rs863224838
Biobank	rs863224838
1000 genomes	rs863224838
hgdp	rs863224838
ensembl	rs863224838
geneview	rs863224838
scholar	rs863224838
google	rs863224838
pharmgkb	rs863224838
gwascentral	rs863224838
openSNP	rs863224838
23andMe	rs863224838
SNPshot	rs863224838
SNPdbe	rs863224838
MSV3d	rs863224838
GWAS Ctlg	rs863224838

Max Magnitude

5

aka c.967delTinsGG (p.Phe323Glyfs)

ClinVar
Risk	rs863224838(GG;GG)
Alt	rs863224838(GG;GG)
Reference	Rs863224838(T;T)
Significance	Pathogenic
Disease	Thrombophilia due to protein S deficiency
Variation	info
Gene	PROS1
CLNDBN	Thrombophilia due to protein S deficiency, autosomal recessive
Reversed	1
HGVS	NC_000003.11:g.93611965delAinsCC
CLNSRC
CLNACC	RCV000197344.1,