List of variants in gene DSP reported as uncertain significance for Primary dilated cardiomyopathy

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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: 22

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.6208G>A (p.Asp2070Asn)	rs41302885	0.00290
NM_004415.4(DSP):c.5178C>A (p.Asn1726Lys)	rs147415451	0.00033
NM_004415.4(DSP):c.273+5G>A	rs200473206	0.00031
NM_004415.4(DSP):c.6307A>G (p.Lys2103Glu)	rs149513743	0.00010
NM_004415.4(DSP):c.5617C>T (p.Arg1873Cys)	rs144392839	0.00009
NM_004415.4(DSP):c.2569G>A (p.Gly857Ser)	rs548695484	0.00005
NM_004415.4(DSP):c.137G>A (p.Gly46Asp)	rs140403872	0.00004
NM_004415.4(DSP):c.2684A>G (p.Tyr895Cys)	rs367752002	0.00004
NM_004415.4(DSP):c.4490G>A (p.Arg1497Gln)	rs727505037	0.00004
NM_004415.4(DSP):c.8117A>T (p.Lys2706Met)	rs537588390	0.00004
NM_004415.4(DSP):c.344A>G (p.Asn115Ser)	rs28763958	0.00003
NM_004415.4(DSP):c.5066T>C (p.Ile1689Thr)	rs869025394	0.00003
NM_004415.4(DSP):c.3973A>C (p.Lys1325Gln)	rs41302883	0.00001
NM_004415.4(DSP):c.8477G>A (p.Arg2826His)	rs548754771	0.00001
NM_004415.4(DSP):c.1067C>A (p.Thr356Lys)	rs780626687
NM_004415.4(DSP):c.1544C>T (p.Pro515Leu)	rs730880079
NM_004415.4(DSP):c.2432T>C (p.Leu811Pro)	rs869025391
NM_004415.4(DSP):c.3346T>C (p.Tyr1116His)	rs1581815394
NM_004415.4(DSP):c.55C>T (p.Arg19Cys)	rs777340009
NM_004415.4(DSP):c.6185A>G (p.His2062Arg)	rs730880086
NM_004415.4(DSP):c.6305G>C (p.Gly2102Ala)	rs572843477
NM_004415.4(DSP):c.7308T>A (p.Asp2436Glu)	rs1581823824

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