List of variants in gene DSP reported as uncertain significance for cardiac rhythm disease

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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_004415.4(DSP):c.889G>A (p.Asp297Asn)	rs201930322	0.00014
NM_004415.4(DSP):c.1483G>A (p.Val495Met)	rs372014020	0.00011
NM_004415.4(DSP):c.3134G>A (p.Arg1045Gln)	rs374263890	0.00004
NM_004415.4(DSP):c.2047G>A (p.Glu683Lys)	rs775181391	0.00003
NM_004415.4(DSP):c.4565C>T (p.Thr1522Met)	rs375150075	0.00002
NM_004415.4(DSP):c.1901C>G (p.Thr634Arg)	rs139964486	0.00001
NM_004415.4(DSP):c.2260G>A (p.Glu754Lys)	rs730880080	0.00001
NM_004415.4(DSP):c.2597G>A (p.Arg866His)	rs764965132	0.00001
NM_004415.4(DSP):c.479G>A (p.Arg160Gln)	rs752941845	0.00001
NM_004415.4(DSP):c.6812A>C (p.Lys2271Thr)	rs730880089	0.00001
NM_004415.4(DSP):c.7249G>T (p.Asp2417Tyr)	rs760501352	0.00001
NM_004415.4(DSP):c.1388T>C (p.Leu463Pro)	rs1758934036
NM_004415.4(DSP):c.7186T>A (p.Tyr2396Asn)	rs863225268

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