List of variants reported as pathogenic for Thrombophilia due to protein S deficiency, autosomal dominant by Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000313.4(PROS1):c.122G>A (p.Arg41His)
NM_000313.4(PROS1):c.1870+1G>C	rs780859898
NM_000313.4(PROS1):c.263G>A (p.Cys88Tyr)
NM_000313.4(PROS1):c.740G>C (p.Cys247Ser)	rs2107158284
NM_000313.4(PROS1):c.76+2_76+3del	rs2107279030

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