List of variants in gene DSPP reported as benign by PreventionGenetics, part of Exact Sciences

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_014208.3(DSPP):c.*17G>A	rs2615489	0.87779
NM_014208.3(DSPP):c.897A>G (p.Ser299=)	rs2736982	0.65063
NM_014208.3(DSPP):c.136-33T>C	rs13131929	0.44289
NM_014208.3(DSPP):c.136-29T>C	rs13131936	0.22261
NM_014208.3(DSPP):c.202A>T (p.Arg68Trp)	rs36094464	0.14530
NM_014208.3(DSPP):c.708T>C (p.Asp236=)	rs61731010	0.04620
NM_014208.3(DSPP):c.727G>A (p.Asp243Asn)	rs3750025	0.04053
NM_014208.3(DSPP):c.303C>T (p.Asn101=)	rs61731008	0.00424
NM_014208.3(DSPP):c.1326T>C (p.Gly442=)	rs117746821	0.00075
NM_014208.3(DSPP):c.1778G>C (p.Ser593Thr)

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