List of variants in gene combination FPGT-TNNI3K, LRRC53, TNNI3K reported as uncertain significance for Atrial 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_015978.3(TNNI3K):c.2157dup (p.Glu720fs)	rs754423974	0.00031
NM_015978.3(TNNI3K):c.2121+7442G>A	rs780599948	0.00005
NM_015978.3(TNNI3K):c.2128C>A (p.Pro710Thr)	rs367667018	0.00004
NM_015978.3(TNNI3K):c.2121+7526_2121+7529dup	rs1416246083	0.00002
NM_015978.3(TNNI3K):c.2309A>T (p.Glu770Val)	rs765132869	0.00002
NM_015978.3(TNNI3K):c.2177T>C (p.Ile726Thr)	rs1279580722	0.00001
NM_015978.3(TNNI3K):c.2269C>T (p.Arg757Trp)	rs201798397	0.00001
NM_001112808.3(FPGT-TNNI3K):c.2508C>A (p.Asn836Lys)	rs199608014
NM_015978.3(TNNI3K):c.2222C>A (p.Ser741Ter)	rs548261851
NM_015978.3(TNNI3K):c.2258G>C (p.Gly753Ala)	rs144507273
NM_015978.3(TNNI3K):c.2297G>C (p.Arg766Pro)	rs201340993

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