Variants in gene KCND3 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_001378969.1(KCND3):c.1456A>G (p.Thr486Ala)	rs149008060	0.00077
NM_001378969.1(KCND3):c.1573A>G (p.Met525Val)	rs145890206	0.00076
NM_001378969.1(KCND3):c.5C>A (p.Ala2Glu)	rs201340369	0.00066
NM_001378969.1(KCND3):c.641A>G (p.Lys214Arg)	rs142744204	0.00034
NM_001378969.1(KCND3):c.1292G>A (p.Arg431His)	rs771703569	0.00015
NM_001378969.1(KCND3):c.1348C>T (p.Leu450Phe)	rs150401343	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.1314G>A (p.Ser438=)	rs1247179970	0.00003
NM_001378969.1(KCND3):c.1370C>T (p.Thr457Met)	rs199637120	0.00003
NM_001378969.1(KCND3):c.1492T>C (p.Leu498=)	rs762528364	0.00001
NM_001378969.1(KCND3):c.186G>A (p.Pro62=)	rs1411627342	0.00001
NM_001378969.1(KCND3):c.1920G>A (p.Thr640=)

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