ClinVar Miner

List of variants reported as benign for Thrombophilia due to protein S deficiency, autosomal dominant by Mendelics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000313.4(PROS1):c.1528G>A (p.Val510Met)	rs138925964	0.00331
NM_000313.4(PROS1):c.76+7A>G	rs201928951	0.00056
NM_000313.4(PROS1):c.119G>T (p.Arg40Leu)	rs7614835

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