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: 11

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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.30C>A (p.Asn10Lys)	rs201692618	0.00042
NM_152594.3(SPRED1):c.376+3A>T	rs775985211	0.00014
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.306G>A (p.Thr102=)	rs372791883	0.00003
NM_152594.3(SPRED1):c.1110C>T (p.Leu370=)	rs876657584
NM_152594.3(SPRED1):c.117A>G (p.Leu39=)	rs2542660979
NM_152594.3(SPRED1):c.207+37A>G	rs2272105
NM_152594.3(SPRED1):c.885T>C (p.Ser295=)	rs1888476496

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