Variants in gene GALE with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001008216.2(GALE):c.284G>A (p.Gly95Asp)	rs1243531358	0.00001
NM_001008216.2(GALE):c.449C>T (p.Thr150Met)	rs765353795	0.00001
NM_001008216.2(GALE):c.658C>T (p.Arg220Trp)	rs764909409	0.00001

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