List of variants in gene SCP2 reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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_002979.5(SCP2):c.974-18C>T	rs7516939	0.32462
NM_002979.5(SCP2):c.987G>T (p.Thr329=)	rs7538935	0.16959
NM_002979.5(SCP2):c.1235+30G>A	rs7529265	0.14185
NM_002979.5(SCP2):c.1236-16A>G	rs17107640	0.13565
NM_002979.5(SCP2):c.609A>G (p.Glu203=)	rs41294530	0.06615
NM_002979.5(SCP2):c.*7C>A	rs10888761	0.05835
NM_002979.5(SCP2):c.1224G>A (p.Pro408=)	rs80253221	0.00680
NM_002979.5(SCP2):c.1468+17C>A	rs79342751	0.00163

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