ClinVar Miner

Submissions for variant NM_000313.3(PROS1):c.1528G>A (p.Val510Met) (rs138925964)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CSER_CC_NCGL; University of Washington Medical Center RCV000148749 SCV000190486 likely benign Protein S deficiency 2014-06-01 no assertion criteria provided research
Invitae RCV000458043 SCV000561929 benign Thrombophilia due to protein S deficiency, autosomal recessive 2016-12-05 criteria provided, single submitter clinical testing
Russ Altman Lab,Stanford University RCV000148749 SCV000298014 risk factor Protein S deficiency 2015-05-01 no assertion criteria provided research

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