List of variants in gene combination CASD1, SGCE 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_003919.3(SGCE):c.391-3T>C	rs17166384	0.08209
NM_003919.3(SGCE):c.369G>C (p.Val123=)	rs140913016	0.00393
NM_003919.3(SGCE):c.410G>A (p.Arg137His)	rs548306335	0.00003
NM_003919.3(SGCE):c.110-9T>C	rs781152122	0.00001
NM_003919.3(SGCE):c.1253+766_1253+767del
NM_003919.3(SGCE):c.1253+799G>A
NM_003919.3(SGCE):c.436T>A (p.Leu146Met)	rs752074255

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