List of variants in gene EHMT1 reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_024757.5(EHMT1):c.1089T>C (p.Gly363=)	rs1129768	0.49865
NM_024757.5(EHMT1):c.444T>C (p.Pro148=)	rs3812497	0.23632
NM_024757.5(EHMT1):c.1044G>A (p.Ser348=)	rs1129767	0.14787
NM_024757.5(EHMT1):c.1368C>T (p.Leu456=)	rs45450992	0.07198
NM_024757.5(EHMT1):c.1369+9C>T	rs146125583	0.00794
NM_024757.5(EHMT1):c.316C>G (p.Gln106Glu)	rs144603232	0.00489
NM_024757.5(EHMT1):c.3016G>A (p.Val1006Met)	rs33999936	0.00183
NM_024757.5(EHMT1):c.2040G>A (p.Ser680=)	rs150451099	0.00146
NM_024757.5(EHMT1):c.2695A>G (p.Ile899Val)	rs144085805	0.00020
NM_024757.5(EHMT1):c.2970G>T (p.Gln990His)	rs143669310	0.00018
NM_024757.5(EHMT1):c.2505+1146T>G
NM_024757.5(EHMT1):c.3375-15CT[2]	rs112664025
NM_024757.5(EHMT1):c.3541-13TC[3]	rs10667884
NM_024757.5(EHMT1):c.432C>T (p.Ala144=)	rs139461232

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