List of variants in gene SPARC reported as benign

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_003118.4(SPARC):c.331-59T>G	rs7719521	0.64754
NM_003118.4(SPARC):c.208+127A>G	rs1864966	0.64683
NM_003118.4(SPARC):c.208+31C>T	rs1978707	0.64663
NM_003118.4(SPARC):c.*582G>C	rs1054204	0.44854
NM_003118.4(SPARC):c.452-69T>G	rs749575	0.25335
NM_003118.4(SPARC):c.120+36T>G	rs2116780	0.17433
NM_003118.4(SPARC):c.66A>G (p.Glu22=)	rs2304052	0.17386
NM_003118.4(SPARC):c.57+56G>C	rs7714314	0.16845
NM_003118.4(SPARC):c.585+100G>A	rs729853	0.16730
NM_003118.4(SPARC):c.121-142G>A	rs17112183	0.09730
NM_003118.4(SPARC):c.-13-281C>T	rs11746883	0.03256
NM_003118.4(SPARC):c.55C>T (p.Pro19Ser)	rs6874468	0.02386
NM_003118.4(SPARC):c.120+8G>T	rs199756185	0.00153
NM_003118.4(SPARC):c.204G>A (p.Ala68=)	rs143533525	0.00018
NM_003118.4(SPARC):c.633C>T (p.His211=)	rs149306790	0.00009
NM_003118.4(SPARC):c.120+42T>C	rs2304051
NM_003118.4(SPARC):c.208+153G>C	rs2304050
NM_003118.4(SPARC):c.209-234C>G	rs6579885
NM_003118.4(SPARC):c.452-332G>A	rs2347126
NM_003118.4(SPARC):c.585+298T>C	rs56916069
NM_003118.4(SPARC):c.586-268G>A	rs6892840

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