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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) 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: 21

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HGVS	dbSNP	gnomAD frequency
NM_000155.4(GALT):c.1006A>T (p.Met336Leu)	rs111033810	0.00004
NM_000155.4(GALT):c.857A>G (p.Tyr286Cys)	rs367543262	0.00003
NM_000155.4(GALT):c.1018G>A (p.Glu340Lys)	rs111033806	0.00001
NM_000155.4(GALT):c.265T>G (p.Tyr89Asp)	rs111033666	0.00001
NM_000155.4(GALT):c.590A>G (p.Asp197Gly)	rs1554709359	0.00001
NM_000155.4(GALT):c.593T>C (p.Ile198Thr)	rs1483461355	0.00001
NM_000155.4(GALT):c.772C>T (p.Arg258Cys)	rs368166217	0.00001
NM_000155.4(GALT):c.814C>T (p.Arg272Cys)	rs111033766	0.00001
NM_000155.4(GALT):c.883C>A (p.Pro295Thr)	rs111033783	0.00001
NM_000155.4(GALT):c.961C>T (p.His321Tyr)	rs367543266	0.00001
NM_000155.4(GALT):c.1049C>A (p.Thr350Asn)	rs775317639
NM_000155.4(GALT):c.329G>A (p.Gly110Glu)	rs1057523885
NM_000155.4(GALT):c.385A>T (p.Met129Leu)	rs193922248
NM_000155.4(GALT):c.394C>T (p.His132Tyr)	rs111033688
NM_000155.4(GALT):c.405G>A (p.Ser135=)	rs141232328
NM_000155.4(GALT):c.547C>A (p.Pro183Thr)	rs111033721
NM_000155.4(GALT):c.552C>A (p.His184Gln)	rs111033717
NM_000155.4(GALT):c.572C>T (p.Ala191Val)	rs794727838
NM_000155.4(GALT):c.776G>A (p.Arg259Gln)	rs886042070
NM_000155.4(GALT):c.812A>G (p.Glu271Gly)	rs111033765
NM_000155.4(GALT):c.893T>C (p.Met298Thr)	rs886042064

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