Variants in gene KBTBD13 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001101362.3(KBTBD13):c.290T>C (p.Leu97Pro)	rs767384093	0.00005
NM_001101362.3(KBTBD13):c.1184C>T (p.Thr395Met)	rs758995387	0.00004
NM_001101362.3(KBTBD13):c.1191G>C (p.Val397=)	rs376673920	0.00004
NM_001101362.3(KBTBD13):c.228C>G (p.Asp76Glu)	rs777431652	0.00003
NM_001101362.3(KBTBD13):c.251G>C (p.Cys84Ser)	rs999785767	0.00002
NM_001101362.3(KBTBD13):c.252C>T (p.Cys84=)	rs886051334	0.00001
NM_001101362.3(KBTBD13):c.162C>T (p.Ser54=)	rs1162054356
NM_001101362.3(KBTBD13):c.309G>C (p.Ser103=)	rs760134475
NM_001101362.3(KBTBD13):c.634_638del (p.Tyr212fs)	rs748327666

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