ClinVar Miner

Submissions for variant NM_000313.4(PROS1):c.815G>A (p.Gly272Glu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Juno Genomics, Hangzhou Juno Genomics, Inc RCV004795554 SCV005416091 uncertain significance Thrombophilia due to protein S deficiency, autosomal dominant; Thrombophilia due to protein S deficiency, autosomal recessive criteria provided, single submitter clinical testing PM2_Supporting+PP3

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