Variants in gene TCTN2 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_024809.5(TCTN2):c.599G>A (p.Arg200Gln)	rs79251326	0.00978
NM_024809.5(TCTN2):c.720C>G (p.Pro240=)	rs149430216	0.00236
NM_024809.5(TCTN2):c.-2G>A	rs141768405	0.00224
NM_024809.5(TCTN2):c.615C>T (p.Gly205=)	rs147485641	0.00143

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