List of variants in gene DSP reported as benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.2091A>G (p.Gly697=)	rs2076304	0.76849
NM_004415.4(DSP):c.8472G>C (p.Gly2824=)	rs2744380	0.68624
NM_004415.4(DSP):c.7122C>T (p.Thr2374=)	rs2076300	0.28306
NM_004415.4(DSP):c.2862C>T (p.Cys954=)	rs2064217	0.27166
NM_004415.4(DSP):c.1dup (p.Met1fs)	rs17133512	0.17362
NM_004415.4(DSP):c.4535A>G (p.Tyr1512Cys)	rs2076299	0.13777
NM_004415.4(DSP):c.126T>C (p.Tyr42=)	rs36087964	0.06956
NM_004415.4(DSP):c.4578C>A (p.Asn1526Lys)	rs28763966	0.04717
NM_004415.4(DSP):c.8175C>A (p.Arg2725=)	rs11558731	0.04375
NM_004415.4(DSP):c.273+10C>T	rs56148603	0.02451
NM_004415.4(DSP):c.4773G>A (p.Arg1591=)	rs28763968	0.01341
NM_004415.4(DSP):c.4455G>T (p.Arg1485Ser)	rs113902911	0.00572
NM_004415.4(DSP):c.6208G>A (p.Asp2070Asn)	rs41302885	0.00290
NM_004415.4(DSP):c.3923G>A (p.Arg1308Gln)	rs184154918	0.00037
NM_004415.4(DSP):c.1557C>T (p.Ala519=)	rs769629611	0.00003

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