List of variants in gene ERCC6 reported as likely 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000124.4(ERCC6):c.135C>G (p.Leu45=)	rs2228524	0.62551
NM_000124.4(ERCC6):c.3637A>G (p.Arg1213Gly)	rs2228527	0.19565
NM_000124.4(ERCC6):c.3289A>G (p.Met1097Val)	rs2228526	0.19072
NM_000124.4(ERCC6):c.4238A>G (p.Gln1413Arg)	rs2228529	0.18890
NM_000124.4(ERCC6):c.411G>A (p.Leu137=)	rs4253013	0.09896
NM_000124.4(ERCC6):c.3177T>C (p.Ser1059=)	rs4253207	0.01168
NM_000124.4(ERCC6):c.4065T>G (p.Asp1355Glu)	rs34917815	0.00246
NM_000124.4(ERCC6):c.2403C>T (p.Ala801=)	rs114896216	0.00234
NM_000124.4(ERCC6):c.3122A>C (p.Gln1041Pro)	rs139007661	0.00179
NM_000124.4(ERCC6):c.4223A>C (p.Glu1408Ala)	rs61760167	0.00154
NM_000124.4(ERCC6):c.150G>A (p.Val50=)	rs80133923	0.00073
NM_000124.4(ERCC6):c.2391C>T (p.Ser797=)	rs142641602	0.00031
NM_000124.4(ERCC6):c.3581A>G (p.Glu1194Gly)	rs114479292	0.00009
NM_000124.4(ERCC6):c.1685+12T>C
NM_000124.4(ERCC6):c.3284C>G (p.Pro1095Arg)	rs4253208
NM_000124.4(ERCC6):c.3689G>C (p.Arg1230Pro)	rs4253211

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