List of variants in gene combination LOC126860875, NEBL 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_006393.3(NEBL):c.2101C>A (p.Pro701Thr)	rs371551337	0.00016
NM_006393.3(NEBL):c.2092A>G (p.Ile698Val)	rs565742208	0.00005
NM_006393.3(NEBL):c.2148+1G>A	rs762179161	0.00003
NM_006393.3(NEBL):c.2104C>T (p.Pro702Ser)	rs780795108	0.00002
NM_006393.3(NEBL):c.2108A>G (p.Glu703Gly)	rs907637021	0.00002
NM_006393.3(NEBL):c.2105C>T (p.Pro702Leu)	rs1838860400	0.00001
NM_006393.3(NEBL):c.2063A>T (p.Tyr688Phe)
NM_006393.3(NEBL):c.2066A>G (p.Lys689Arg)	rs1838865198
NM_006393.3(NEBL):c.2110C>G (p.Leu704Val)	rs751282061
NM_006393.3(NEBL):c.2122A>C (p.Lys708Gln)
NM_006393.3(NEBL):c.2147A>G (p.Asn716Ser)
NM_006393.3(NEBL):c.2148+2T>A
NM_213569.2(NEBL):c.358-4751_358-4740del	rs2130816665

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