List of variants in gene DDC reported as likely 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001082971.2(DDC):c.782-283A>G	rs11575388	0.02336
NM_001082971.2(DDC):c.315+260T>A	rs11575309	0.02269
NM_001082971.2(DDC):c.944+63G>A	rs4947580	0.01799
NM_001082971.2(DDC):c.-28-56C>T	rs3779076	0.01789
NM_001082971.2(DDC):c.-28-201C>G	rs3779075	0.01787
NM_001082971.2(DDC):c.876+129A>G	rs11575392	0.01396
NM_001082971.2(DDC):c.570+284A>G	rs11575339	0.01377
NM_001082971.2(DDC):c.201+37A>G	rs11575293	0.01073
NM_001082971.2(DDC):c.435+61C>T	rs11575319	0.01072
NM_001082971.2(DDC):c.1042-291G>T	rs11575493	0.01056
NM_001082971.2(DDC):c.1243-138C>T	rs11575541	0.01056
NM_001082971.2(DDC):c.1042-111G>A	rs112093238	0.00691
NM_001082971.2(DDC):c.1021+122C>A	rs115760747
NM_001082971.2(DDC):c.945-252C>G	rs11575454

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