List of variants in gene DSPP reported as likely pathogenic for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014208.3(DSPP):c.2525del (p.Ser842fs)	rs1395922945	0.00002
NM_014208.3(DSPP):c.1282_1283del (p.Gln428fs)
NM_014208.3(DSPP):c.52-1G>C	rs1057521972

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