Variants in gene CACNA1F 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001256789.3(CACNA1F):c.1870G>A (p.Val624Ile)	rs141010716	0.00227
NM_001256789.3(CACNA1F):c.2764G>A (p.Gly922Ser)	rs149685267	0.00086
NM_001256789.3(CACNA1F):c.904C>T (p.Arg302Cys)	rs139612152	0.00032
NM_001256789.3(CACNA1F):c.3236+3G>A	rs199932603	0.00019
NM_001256789.3(CACNA1F):c.761T>C (p.Ile254Thr)	rs202029187	0.00018
NM_001256789.3(CACNA1F):c.3833G>A (p.Arg1278His)	rs782330306	0.00014
NM_001256789.3(CACNA1F):c.5827G>A (p.Asp1943Asn)	rs374663693	0.00009
NM_001256789.3(CACNA1F):c.1156G>A (p.Gly386Arg)	rs782315613	0.00007
NM_001256789.3(CACNA1F):c.2777G>A (p.Arg926His)	rs782092924	0.00005
NM_001256789.3(CACNA1F):c.5232G>A (p.Arg1744=)	rs782598962	0.00005
NM_001256789.3(CACNA1F):c.91G>A (p.Gly31Arg)	rs782426237	0.00005
NM_001256789.3(CACNA1F):c.209G>A (p.Arg70Gln)	rs781923569	0.00003
NM_001256789.3(CACNA1F):c.5563G>A (p.Gly1855Ser)	rs367608150	0.00003
NM_001256789.3(CACNA1F):c.2444G>T (p.Gly815Val)	rs781938466	0.00002
NM_001256789.3(CACNA1F):c.5332C>T (p.Arg1778Cys)	rs781892709	0.00002
NM_001256789.3(CACNA1F):c.2415AGAGGAAGA[2] (p.Glu812_Glu814del)	rs59355923
NM_001256789.3(CACNA1F):c.2415AGAGGAAGA[4] (p.Glu812_Glu814dup)	rs59355923

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