List of variants in gene EMD reported as likely benign by Invitae

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 7

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HGVS	dbSNP
NM_000117.2(EMD):c.12C>T (p.Tyr4=)	rs782011714
NM_000117.2(EMD):c.315T>C (p.Tyr105=)	rs1342409944
NM_000117.2(EMD):c.466G>A (p.Gly156Ser)	rs144594695
NM_000117.2(EMD):c.489C>T (p.Ser163=)	rs782558454
NM_000117.2(EMD):c.495G>A (p.Thr165=)	rs151074632
NM_000117.2(EMD):c.525C>T (p.Ser175=)	rs782367505
NM_000117.2(EMD):c.57C>T (p.Tyr19=)	rs371661299

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