List of variants in gene PDE1A reported as benign by GeneDx

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_001363871.4(PDE1A):c.168-1739A>C	rs2568667	0.71369
NM_001363871.4(PDE1A):c.168-1408G>C	rs2623435	0.71289
NM_001363871.4(PDE1A):c.168-1978C>A	rs2170403	0.71274
NM_001363871.4(PDE1A):c.776+7C>T	rs3754929	0.68905
NC_000002.12:g.182522885T>C	rs2303890	0.33593
NM_001363871.4(PDE1A):c.902+48T>A	rs1344773	0.29780
NM_001363871.4(PDE1A):c.777-119C>T	rs55747252	0.27547
NM_001363871.4(PDE1A):c.1516+17417T>C	rs2276612	0.27360
NM_001363871.4(PDE1A):c.54-101T>C	rs10930999	0.22605
NM_001363871.4(PDE1A):c.1208-134A>G	rs10930991	0.20446
NM_001363871.4(PDE1A):c.1207+48G>C	rs3769796	0.18845
NM_001363871.4(PDE1A):c.167+202A>G	rs3769779	0.10034
NM_005019.7(PDE1A):c.101+113C>T	rs67483153	0.06697
NM_001363871.4(PDE1A):c.168-1806A>G	rs6740124	0.05501
NM_001363871.4(PDE1A):c.1207+62A>T	rs10497595	0.03443
NM_001363871.4(PDE1A):c.902+87C>T	rs74397875	0.03363
NM_001363871.4(PDE1A):c.1004+24G>T	rs200353420	0.03293
NM_001363871.4(PDE1A):c.1516+17841A>G	rs78879279	0.03265
NM_001363871.4(PDE1A):c.534+233T>C	rs16822903	0.01793
NM_001363871.4(PDE1A):c.675+60T>G	rs73977312	0.00462
NM_001363871.4(PDE1A):c.1004+32_1004+37dup	rs56413404
NM_001363871.4(PDE1A):c.1004+33_1004+37dup	rs56413404
NM_001363871.4(PDE1A):c.1004+35_1004+37dup	rs56413404
NM_001363871.4(PDE1A):c.1004+36_1004+37dup	rs56413404
NM_001363871.4(PDE1A):c.1004+37dup	rs56413404
NM_001363871.4(PDE1A):c.1208-106T>C	rs7597711
NM_001363871.4(PDE1A):c.1329-157G>C	rs1368216
NM_001363871.4(PDE1A):c.1516+17598del	rs78156757
NM_001363871.4(PDE1A):c.54-8dup	rs201506982
NM_001363871.4(PDE1A):c.675+224_675+225insAG	rs536517378
NM_001363871.4(PDE1A):c.675+225del	rs10716042

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