List of variants in gene combination LOC110121269, SCN5A reported as not provided for heart conduction 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.2989G>A (p.Ala997Thr)	rs137854609	0.00008
NM_000335.5(SCN5A):c.3068G>A (p.Arg1023His)	rs199473592	0.00006
NM_000335.5(SCN5A):c.2893C>T (p.Arg965Cys)	rs199473180	0.00001
NM_000335.5(SCN5A):c.3335C>T (p.Ala1112Val)	rs199473194	0.00001
NM_000335.5(SCN5A):c.2804T>C (p.Leu935Pro)	rs199473179
NM_000335.5(SCN5A):c.2894G>A (p.Arg965His)	rs199473181
NM_000335.5(SCN5A):c.3164A>G (p.Asp1055Gly)	rs199473593
NM_000335.5(SCN5A):c.3233C>A (p.Ser1078Tyr)	rs199473188

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