List of variants in gene SNTA1 reported as 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.909+30T>C	rs291694	0.69088
NM_003098.3(SNTA1):c.496+297G>C	rs3764672	0.42363
NM_003098.3(SNTA1):c.1238-129C>T	rs112108236	0.02251
NM_003098.3(SNTA1):c.807T>C (p.Asn269=)	rs73270015	0.02196
NM_003098.3(SNTA1):c.1237+158T>C	rs142832155	0.01774
NM_003098.3(SNTA1):c.497-264A>G	rs114498974	0.01763
NM_003098.3(SNTA1):c.1426-50G>A	rs77750269	0.01614
NM_003098.3(SNTA1):c.1350C>T (p.Phe450=)	rs116747979	0.01203
NM_003098.3(SNTA1):c.828G>A (p.Lys276=)	rs35938843	0.00969
NM_003098.3(SNTA1):c.555C>T (p.Val185=)	rs34995247	0.00948
NM_003098.3(SNTA1):c.317G>A (p.Arg106Gln)	rs75025585	0.00904
NM_003098.3(SNTA1):c.701+10G>A	rs6057846	0.00419
NM_003098.3(SNTA1):c.770C>G (p.Ala257Gly)	rs56157422	0.00217
NM_003098.3(SNTA1):c.497-7C>T	rs116972153	0.00063
NM_003098.3(SNTA1):c.*79C>A	rs78892511	0.00040
NM_003098.3(SNTA1):c.*231C>T	rs187657721	0.00018
NM_003098.3(SNTA1):c.1238-14T>C	rs369876616	0.00006
NM_003098.3(SNTA1):c.1158G>A (p.Pro386=)	rs774320273	0.00004
NM_003098.3(SNTA1):c.*122G>A	rs116151218

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