List of variants in gene ENG 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: 18

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HGVS	dbSNP	gnomAD frequency
NC_000009.12:g.127854979T>G	rs4836586	0.99091
NM_001114753.3(ENG):c.219+25G>T	rs7847860	0.06245
NM_001114753.3(ENG):c.68-215T>C	rs11789912	0.03711
NM_001114753.3(ENG):c.991+58A>T	rs12002508	0.01910
NM_001114753.3(ENG):c.360+21C>T	rs41355248	0.01861
NM_001114753.3(ENG):c.572G>A (p.Gly191Asp)	rs41322046	0.01000
NM_001114753.3(ENG):c.1932C>T (p.Ile644=)	rs181330955	0.00609
NM_001114753.3(ENG):c.225G>A (p.Pro75=)	rs116146060	0.00091
NM_001114753.3(ENG):c.392C>T (p.Pro131Leu)	rs139398993	0.00077
NM_001114753.3(ENG):c.234G>A (p.Leu78=)	rs115675061	0.00076
NM_001114753.3(ENG):c.159C>T (p.Cys53=)	rs148475405	0.00056
NM_001114753.3(ENG):c.219+23G>A	rs200726108	0.00037
NM_001114753.3(ENG):c.-70C>T	rs562538400	0.00020
NM_001114753.3(ENG):c.596G>A (p.Arg199His)	rs548424658	0.00004
NM_001114753.3(ENG):c.*431T>G	rs549011956	0.00001
NM_001114753.3(ENG):c.219+259dup	rs148797940
NM_001114753.3(ENG):c.361-311GA[4]	rs150688809
NM_001114753.3(ENG):c.909C>T (p.Ala303=)	rs200306464

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