List of variants in gene PDYN reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_024411.5(PDYN):c.575A>T (p.Glu192Val)	rs45469293	0.00742
NM_024411.5(PDYN):c.*1071G>A	rs752953257	0.00129
NM_024411.5(PDYN):c.*231C>G	rs565210312	0.00049
NM_024411.5(PDYN):c.*760G>C	rs767631485

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