List of variants in gene PROS1 reported as benign for hematologic disorder

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

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_000313.4(PROS1):c.*520A>C	rs9681204	0.79141
NM_000313.4(PROS1):c.76+4007C>T	rs13062355	0.45865
NM_000313.4(PROS1):c.2001A>G (p.Pro667=)	rs6123	0.33781
NM_000313.4(PROS1):c.1032C>T (p.Ile344=)	rs78449232	0.00981
NM_000313.4(PROS1):c.728-20G>A	rs78230833	0.00438
NM_000313.4(PROS1):c.1528G>A (p.Val510Met)	rs138925964	0.00331
NM_000313.4(PROS1):c.1021G>A (p.Ala341Thr)	rs189883848	0.00312
NM_000313.4(PROS1):c.227C>T (p.Pro76Leu)	rs73846070	0.00238
NM_000313.4(PROS1):c.698G>A (p.Arg233Lys)	rs41267007	0.00202
NM_000313.4(PROS1):c.1095T>G (p.Asn365Lys)	rs199469491	0.00155
NM_000313.4(PROS1):c.234+5G>A	rs187264712	0.00118
NM_000313.4(PROS1):c.76+7A>G	rs201928951	0.00056
NM_000313.4(PROS1):c.1762A>G (p.Thr588Ala)	rs142846443	0.00043
NM_000313.4(PROS1):c.1494T>C (p.Asn498=)	rs76877671	0.00033
NM_000313.4(PROS1):c.431C>A (p.Thr144Asn)	rs146366248	0.00029
NM_000313.4(PROS1):c.1377A>G (p.Gly459=)	rs371312357	0.00012
NM_000313.4(PROS1):c.684C>T (p.Cys228=)	rs377173471	0.00009
NM_000313.4(PROS1):c.1446C>T (p.Gly482=)	rs535201753	0.00003
NM_000313.4(PROS1):c.48C>A (p.Leu16=)	rs559292587	0.00002
NM_000313.4(PROS1):c.1155+4C>G	rs548576399
NM_000313.4(PROS1):c.119G>T (p.Arg40Leu)	rs7614835
NM_000313.4(PROS1):c.1713A>G (p.Gln571=)	rs571916140
NM_000313.4(PROS1):c.470-11dup
NM_000313.4(PROS1):c.965+17A>C

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