List of variants in gene DST reported as benign for not specified

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001374736.1(DST):c.16308G>A (p.Met5436Ile)	rs4715630	0.79707
NM_001374736.1(DST):c.16045A>G (p.Thr5349Ala)	rs4715631	0.68618
NM_001723.7(DST):c.6031G>C (p.Val2011Leu)	rs6459166	0.42446
NM_001723.7(DST):c.4074G>A (p.Lys1358=)	rs2230862	0.40815
NM_001374736.1(DST):c.14068+5G>A	rs9367689	0.38646
NM_001374736.1(DST):c.11792A>G (p.Gln3931Arg)	rs4712138	0.37552
NM_001723.7(DST):c.7765A>G (p.Ile2589Val)	rs150191284	0.02534
NM_001723.7(DST):c.3809A>G (p.Lys1270Arg)	rs35497571	0.02037
NM_001374736.1(DST):c.20997G>A (p.Leu6999=)	rs187652380	0.00781
NM_001374736.1(DST):c.3557G>A (p.Ser1186Asn)	rs139350480	0.00572
NM_001723.7(DST):c.5780A>G (p.His1927Arg)	rs12209266	0.00441
NM_001374736.1(DST):c.2256A>T (p.Ser752=)	rs113432929	0.00225
NM_001374736.1(DST):c.5059-17C>G	rs190803185	0.00089
NM_001374736.1(DST):c.23228G>A (p.Arg7743Gln)	rs762220017	0.00004
NM_001374736.1(DST):c.3126G>A (p.Lys1042=)	rs76795414	0.00004

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