List of variants in gene SPRED1 reported as benign by Genome Diagnostics Laboratory, The Hospital for Sick Children

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_152594.3(SPRED1):c.-93C>T	rs192699510	0.00724
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala)	rs114636635	0.00188
NM_152594.3(SPRED1):c.675C>T (p.Ser225=)	rs144764225	0.00092
NM_152594.3(SPRED1):c.939G>A (p.Thr313=)	rs140644874	0.00070
NM_152594.3(SPRED1):c.30C>A (p.Asn10Lys)	rs201692618	0.00042
NM_152594.3(SPRED1):c.124G>A (p.Val42Ile)	rs147204964	0.00017
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val)	rs200157475	0.00010
NM_152594.3(SPRED1):c.290A>G (p.Lys97Arg)	rs556636985	0.00007
NM_152594.3(SPRED1):c.634G>A (p.Val212Ile)	rs769630742	0.00004
NM_152594.3(SPRED1):c.1225G>T (p.Ala409Ser)	rs762735151	0.00003
NM_152594.3(SPRED1):c.1226C>T (p.Ala409Val)	rs751260227	0.00003
NM_152594.3(SPRED1):c.879G>A (p.Leu293=)	rs535687467	0.00002
NM_152594.3(SPRED1):c.1046G>C (p.Arg349Thr)	rs1221405249	0.00001

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