List of variants in gene GUCY2D reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000180.4(GUCY2D):c.1093C>T (p.Arg365Trp)	rs138836357	0.00069
NM_000180.4(GUCY2D):c.1979G>A (p.Arg660Gln)	rs61750162	0.00013
NM_000180.4(GUCY2D):c.1618C>T (p.Arg540Cys)	rs61749754	0.00002
NM_000180.4(GUCY2D):c.1996C>T (p.Arg666Trp)	rs757387072	0.00001
NM_000180.4(GUCY2D):c.2620G>A (p.Glu874Lys)	rs1001538483	0.00001
NM_000180.4(GUCY2D):c.129_134del (p.Leu44_Leu45del)	rs552184470
NM_000180.4(GUCY2D):c.2849C>T (p.Ala950Val)	rs61750181
NM_000180.4(GUCY2D):c.514C>T (p.Leu172Phe)

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