List of variants in gene GPD1L reported as benign for Brugada syndrome

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_015141.4(GPD1L):c.408C>T (p.Asp136=)	rs9835387	0.17620
NM_015141.4(GPD1L):c.959+16G>A	rs72546643	0.01970
NM_015141.4(GPD1L):c.366+8G>A	rs72546650	0.00621
NM_015141.4(GPD1L):c.396G>A (p.Lys132=)	rs61741845	0.00618
NM_015141.4(GPD1L):c.573C>G (p.Thr191=)	rs72558073	0.00545
NM_015141.4(GPD1L):c.81T>C (p.Asn27=)	rs34278284	0.00515
NM_015141.4(GPD1L):c.370A>G (p.Ile124Val)	rs72552293	0.00291
NM_015141.4(GPD1L):c.981G>A (p.Val327=)	rs144877595	0.00195
NM_015141.4(GPD1L):c.465C>T (p.Ala155=)	rs113645050	0.00121
NM_015141.4(GPD1L):c.619-9C>G	rs2044880	0.00057
NM_015141.4(GPD1L):c.828C>T (p.Ala276=)	rs200392121	0.00055
NM_015141.4(GPD1L):c.813G>T (p.Arg271=)	rs35464343	0.00031
NM_015141.4(GPD1L):c.852+20C>T	rs189819292	0.00001
NM_015141.4(GPD1L):c.618+19dup

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