List of variants in gene PSAP reported as 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_002778.4(PSAP):c.1540-34C>T	rs4747202	0.13788
NM_002778.4(PSAP):c.1005+18C>T	rs55829339	0.13764
NM_002778.4(PSAP):c.-4C>T	rs2070188	0.12811
NM_002778.4(PSAP):c.909+32G>T	rs41307569	0.06451
NM_002778.4(PSAP):c.-10A>G	rs76455588	0.01197
NM_002778.4(PSAP):c.204C>T (p.Asp68=)	rs143981174	0.00484
NM_002778.4(PSAP):c.1380C>T (p.Pro460=)	rs1049882	0.00284
NM_002778.4(PSAP):c.1005+42C>G	rs111759923
NM_002778.4(PSAP):c.1193-26G>A	rs3747860

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