List of variants in gene SPARC reported as uncertain significance for Inborn genetic diseases

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_003118.4(SPARC):c.733G>A (p.Gly245Arg)	rs41290587	0.00445
NM_003118.4(SPARC):c.209A>G (p.Asn70Ser)	rs13359508	0.00230
NM_003118.4(SPARC):c.419A>G (p.Lys140Arg)	rs200223394	0.00006
NM_003118.4(SPARC):c.652C>T (p.Arg218Trp)	rs150910656	0.00005
NM_003118.4(SPARC):c.307G>T (p.Ala103Ser)	rs148618359	0.00004
NM_003118.4(SPARC):c.314T>C (p.Ile105Thr)	rs771396512	0.00003
NM_003118.4(SPARC):c.37G>A (p.Gly13Arg)	rs754061225	0.00003
NM_003118.4(SPARC):c.454A>G (p.Ile152Val)	rs887258352	0.00003
NM_003118.4(SPARC):c.238G>A (p.Gly80Ser)	rs752349310	0.00001
NM_003118.4(SPARC):c.323T>A (p.Phe108Tyr)	rs1760749085	0.00001
NM_003118.4(SPARC):c.343G>T (p.Asp115Tyr)	rs780811976	0.00001
NM_003118.4(SPARC):c.460C>G (p.Pro154Ala)	rs749186030	0.00001
NM_003118.4(SPARC):c.536A>T (p.Tyr179Phe)
NM_003118.4(SPARC):c.601G>A (p.Glu201Lys)	rs1760624090
NM_003118.4(SPARC):c.633C>G (p.His211Gln)
NM_003118.4(SPARC):c.649G>A (p.Ala217Thr)
NM_003118.4(SPARC):c.661G>A (p.Glu221Lys)

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