List of variants in gene PDYN reported as benign by Athena Diagnostics Inc

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_024411.5(PDYN):c.600T>C (p.His200=)	rs6045819	0.16142
NM_024411.5(PDYN):c.575A>T (p.Glu192Val)	rs45469293	0.00742
NM_024411.5(PDYN):c.436A>C (p.Met146Leu)	rs77155664	0.00698
NM_024411.5(PDYN):c.712A>G (p.Thr238Ala)	rs112907294	0.00321
NM_024411.5(PDYN):c.121A>G (p.Asn41Asp)	rs59191035	0.00258
NM_024411.5(PDYN):c.40A>G (p.Met14Val)	rs78675761	0.00108
NM_024411.5(PDYN):c.106G>T (p.Gly36Cys)	rs149056587	0.00067
NM_024411.5(PDYN):c.67C>T (p.Leu23=)	rs77727400	0.00029
NM_024411.5(PDYN):c.732G>A (p.Pro244=)	rs141248791	0.00016
NM_024411.5(PDYN):c.716G>A (p.Arg239Gln)	rs185551108	0.00014
NM_024411.5(PDYN):c.268G>A (p.Gly90Arg)	rs201585283	0.00006
NM_024411.5(PDYN):c.72G>A (p.Ser24=)	rs745951521	0.00001
NM_024411.5(PDYN):c.582C>T (p.Asp194=)	rs769461186

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