List of variants in gene PDYN reported as uncertain significance for not specified

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024411.5(PDYN):c.-19-1G>C	rs769835663	0.00010
NM_024411.5(PDYN):c.583G>A (p.Gly195Arg)	rs766877230	0.00003
NM_024411.5(PDYN):c.34del (p.Leu12fs)	rs761385412
NM_024411.5(PDYN):c.394G>T (p.Gly132Cys)	rs1430436485
NM_024411.5(PDYN):c.658_659del (p.Trp220fs)	rs748307861
NM_024411.5(PDYN):c.80C>G (p.Ser27Cys)	rs536626217

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