Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906675
rs387906675
PROS1
0.800 GeneticVariation UNIPROT Intracerebral mass bleeding in a term neonate: manifestation of hereditary protein S deficiency with a new mutation in the PROS1 gene. 20484936

2010
dbSNP: rs387906675
rs387906675
PROS1
C 0.800 CausalMutation CLINVAR

dbSNP: rs6122
rs6122
PROS1
A 0.700 GeneticVariation CLINVAR Genotype and laboratory and clinical phenotypes of protein s deficiency. 22261441

2012
dbSNP: rs6122
rs6122
PROS1
A 0.700 GeneticVariation CLINVAR Protein S inherited qualitative deficiency: novel mutations and phenotypic influence. 20880255

2010
dbSNP: rs6122
rs6122
PROS1
A 0.700 GeneticVariation CLINVAR Protein S Gla-domain mutations causing impaired Ca(2+)-induced phospholipid binding and severe functional protein S deficiency. 12351389

2002
dbSNP: rs6122
rs6122
PROS1
A 0.700 GeneticVariation CLINVAR Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene. 7803790

1995
dbSNP: rs1241365457
rs1241365457
PROS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1559926604
rs1559926604
PROS1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs759677822
rs759677822
PROS1
G 0.700 CausalMutation CLINVAR

dbSNP: rs863224838
rs863224838
PROS1
CC 0.700 CausalMutation CLINVAR