List of variants in gene SPRED1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_152594.3(SPRED1):c.675C>T (p.Ser225=)	rs144764225	0.00092
NM_152594.3(SPRED1):c.702C>G (p.Ile234Met)	rs138553244	0.00074
NM_152594.3(SPRED1):c.376+3A>T	rs775985211	0.00015
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val)	rs200157475	0.00010
NM_152594.3(SPRED1):c.634G>A (p.Val212Ile)	rs769630742	0.00004
NM_152594.3(SPRED1):c.117A>G (p.Leu39=)
NM_152594.3(SPRED1):c.207+37A>G	rs2272105
NM_152594.3(SPRED1):c.885T>C (p.Ser295=)

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