List of variants in gene PCCA 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000282.4(PCCA):c.914+19A>G	rs4306370	0.92464
NM_000282.4(PCCA):c.1644-31A>G	rs9518061	0.66246
NM_000282.4(PCCA):c.627A>G (p.Ala209=)	rs538229	0.14245
NM_000282.4(PCCA):c.1745C>T (p.Ser582Leu)	rs16957356	0.01499
NM_000282.4(PCCA):c.1429+7A>G	rs16957276	0.01356
NM_000282.4(PCCA):c.1846-9G>T	rs141118743	0.00627
NM_000282.4(PCCA):c.24A>G (p.Thr8=)	rs117397004	0.00013
NM_000282.4(PCCA):c.1285-13_1285-6del	rs535982202
NM_000282.4(PCCA):c.184-17_184-16del	rs111778723
NM_000282.4(PCCA):c.231+47_231+50del	rs147037340

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