Variants in gene FIG4 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_014845.6(FIG4):c.122T>C (p.Ile41Thr)	rs121908287	0.00117
NM_014845.6(FIG4):c.834A>T (p.Lys278Asn)	rs138048706	0.00029
NM_014845.6(FIG4):c.1940A>G (p.Tyr647Cys)	rs150301327	0.00008
NM_014845.6(FIG4):c.1583+3A>G	rs866431185
NM_014845.6(FIG4):c.2097-10C>G	rs142482745
NM_014845.6(FIG4):c.2547-5T>G	rs200267243
NM_014845.6(FIG4):c.640G>A (p.Gly214Arg)	rs529048339

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