List of variants in gene KCND3 reported as uncertain significance for heart conduction disease

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001378969.1(KCND3):c.1292G>A (p.Arg431His)	rs771703569	0.00015
NM_001378969.1(KCND3):c.1702C>T (p.Arg568Cys)	rs144120746	0.00011
NM_001378969.1(KCND3):c.1889G>A (p.Arg630Gln)	rs774713377	0.00006
NM_001378969.1(KCND3):c.1798G>A (p.Gly600Arg)	rs149344567	0.00005
NM_001378969.1(KCND3):c.1649G>A (p.Arg550His)	rs151164490	0.00004
NM_001378969.1(KCND3):c.1370C>T (p.Thr457Met)	rs199637120	0.00003
NM_001378969.1(KCND3):c.1946T>C (p.Val649Ala)	rs760907112	0.00002
NM_001378969.1(KCND3):c.1371G>A (p.Thr457=)	rs773858454	0.00001
NM_001378969.1(KCND3):c.1879G>A (p.Gly627Arg)	rs372362132	0.00001
NM_001378969.1(KCND3):c.346G>A (p.Asp116Asn)	rs766584545	0.00001
NM_001378969.1(KCND3):c.1174G>A (p.Val392Ile)	rs786205867
NM_001378969.1(KCND3):c.1496C>G (p.Ser499Cys)	rs976664434
NM_001378969.1(KCND3):c.1600C>A (p.Pro534Thr)	rs1447493103
NM_001378969.1(KCND3):c.1756C>G (p.Leu586Val)	rs778053688
NM_001378969.1(KCND3):c.1856C>T (p.Thr619Ile)
NM_001378969.1(KCND3):c.817G>A (p.Gly273Ser)	rs869025444

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