List of variants in gene GUCY2D reported as likely benign for not provided

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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: 24

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HGVS	dbSNP	gnomAD frequency
NM_000180.4(GUCY2D):c.154G>T (p.Ala52Ser)	rs61749665	0.29501
NM_000180.4(GUCY2D):c.61T>C (p.Trp21Arg)	rs9905402	0.09880
NM_000180.4(GUCY2D):c.2101C>T (p.Pro701Ser)	rs34598902	0.03505
NM_000180.4(GUCY2D):c.1463+39G>A	rs112984002	0.02392
NM_000180.4(GUCY2D):c.3225-7C>T	rs79887212	0.02045
NM_000180.4(GUCY2D):c.3297G>A (p.Pro1099=)	rs142351773	0.02033
NM_000180.4(GUCY2D):c.1119G>A (p.Val373=)	rs56034424	0.01951
NM_000180.4(GUCY2D):c.1956+21G>T	rs139731548	0.01923
NM_000180.4(GUCY2D):c.2517G>A (p.Thr839=)	rs56316238	0.01492
NM_000180.4(GUCY2D):c.369C>T (p.Gly123=)	rs529594203	0.00117
NM_000180.4(GUCY2D):c.1236C>T (p.Asp412=)	rs61749678	0.00095
NM_000180.4(GUCY2D):c.164C>T (p.Thr55Met)	rs201414567	0.00047
NM_000180.4(GUCY2D):c.921C>T (p.Ala307=)	rs148136213	0.00031
NM_000180.4(GUCY2D):c.1938C>T (p.Leu646=)	rs201196538	0.00025
NM_000180.4(GUCY2D):c.271G>C (p.Ala91Pro)	rs573367793	0.00005
NM_000180.4(GUCY2D):c.3282G>A (p.Leu1094=)	rs281865413	0.00004
NM_000180.4(GUCY2D):c.1518C>T (p.Thr506=)	rs779132852	0.00002
NM_000180.4(GUCY2D):c.3273A>G (p.Arg1091=)	rs375105072	0.00002
NM_000180.4(GUCY2D):c.1008T>C (p.Ser336=)	rs2151799778
NM_000180.4(GUCY2D):c.129_134del (p.Leu44_Leu45del)	rs552184470
NM_000180.4(GUCY2D):c.2113+34G>A
NM_000180.4(GUCY2D):c.2784G>A (p.Gly928=)
NM_000180.4(GUCY2D):c.3009C>T (p.Val1003=)	rs1322441705
NM_000180.4(GUCY2D):c.3043+11C>T	rs116870332

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