List of variants in gene GYG1 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_004130.4(GYG1):c.608+256A>G	rs76917162	0.02746
NM_004130.4(GYG1):c.481+3056C>T	rs34163646	0.02650
NM_004130.4(GYG1):c.482-123C>T	rs559513486	0.00723
NM_004130.4(GYG1):c.481+149del	rs541095432	0.00642
NM_004130.4(GYG1):c.143+111T>C	rs114704879	0.00547
NM_004130.4(GYG1):c.481+3331T>C	rs141510916	0.00400
NM_004130.4(GYG1):c.608+219G>T	rs183245439	0.00384
NM_004130.4(GYG1):c.608+193G>A	rs114395753	0.00379
NM_004130.4(GYG1):c.608+14G>C	rs200902926	0.00366
NM_004130.4(GYG1):c.98G>A (p.Arg33Lys)	rs146101365	0.00128
NM_004130.4(GYG1):c.144-29G>A	rs143942810	0.00044
NM_004130.4(GYG1):c.60G>A (p.Leu20=)	rs145419359	0.00026
NM_004130.4(GYG1):c.143+11C>T	rs367745695	0.00005
NM_004130.4(GYG1):c.609-14C>T	rs199593097	0.00003
NM_004130.4(GYG1):c.267C>T (p.Cys89=)	rs1057521350	0.00001
NM_004130.4(GYG1):c.481+149A>G	rs535827590
NM_004130.4(GYG1):c.481+149_481+153del	rs1256068538
NM_004130.4(GYG1):c.481+151TG[18]	rs10571382
NM_004130.4(GYG1):c.608+289T>G	rs34744953
NM_004130.4(GYG1):c.801C>A (p.Val267=)	rs754894347
NM_004130.4(GYG1):c.897C>T (p.Ala299=)	rs1553733699

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