List of variants in gene PRKCSH 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_001289104.2(PRKCSH):c.822C>T (p.Ala274=)	rs112495629	0.00096
NM_001289104.2(PRKCSH):c.930G>A (p.Ser310=)	rs147897290	0.00049
NM_001289104.2(PRKCSH):c.628G>A (p.Glu210Lys)	rs200168017	0.00039
NM_001289104.2(PRKCSH):c.324C>T (p.Ser108=)	rs368596083	0.00001
NM_001289104.2(PRKCSH):c.1386C>T (p.Pro462=)
NM_001289104.2(PRKCSH):c.1545G>A (p.Thr515=)
NM_001289104.2(PRKCSH):c.1569G>A (p.Pro523=)
NM_001289104.2(PRKCSH):c.156C>T (p.Asn52=)
NM_001289104.2(PRKCSH):c.405C>T (p.Arg135=)	rs746346745
NM_001289104.2(PRKCSH):c.861C>T (p.Thr287=)
NM_001289104.2(PRKCSH):c.939GGA[9] (p.Glu325del)	rs3217229

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