Variants in gene HGSNAT 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_152419.3(HGSNAT):c.1843G>A (p.Ala615Thr)	rs112029032	0.00361
NM_152419.3(HGSNAT):c.1880A>G (p.Tyr627Cys)	rs192857413	0.00082
NM_152419.3(HGSNAT):c.342C>T (p.Asn114=)	rs184883937	0.00077
NM_152419.3(HGSNAT):c.1272C>T (p.Gly424=)	rs147251143	0.00019
NM_152419.3(HGSNAT):c.741G>A (p.Arg247=)	rs775663094	0.00009
NM_152419.3(HGSNAT):c.710C>A (p.Pro237Gln)	rs727503962

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