List of variants in gene PROS1 reported as likely benign for Thrombophilia due to protein S deficiency, autosomal dominant

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000313.4(PROS1):c.*197C>T	rs182088150	0.01026
NM_000313.4(PROS1):c.1032C>T (p.Ile344=)	rs78449232	0.00981
NM_000313.4(PROS1):c.1528G>A (p.Val510Met)	rs138925964	0.00331
NM_000313.4(PROS1):c.-62T>G	rs556711298	0.00328
NM_000313.4(PROS1):c.*992T>G	rs538711279	0.00263
NM_000313.4(PROS1):c.*454G>A	rs539871594	0.00256
NM_000313.4(PROS1):c.698G>A (p.Arg233Lys)	rs41267007	0.00202
NM_000313.4(PROS1):c.*469A>C	rs147496684	0.00164
NM_000313.4(PROS1):c.*380A>T	rs138546241	0.00133
NM_000313.4(PROS1):c.1494T>C (p.Asn498=)	rs76877671	0.00033
NM_000313.4(PROS1):c.1446C>T (p.Gly482=)	rs535201753	0.00003
NM_000313.4(PROS1):c.119G>T (p.Arg40Leu)	rs7614835

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