List of variants reported as likely benign for partial deletion of the long arm of chromosome 7

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_032951.3(MLXIPL):c.1096T>C (p.Leu366=)	rs190197045	0.00595
NM_032951.3(MLXIPL):c.1537G>A (p.Ala513Thr)	rs200391124	0.00214
NM_000501.4(ELN):c.1909G>A (p.Ala637Thr)	rs536177240	0.00026
NM_000501.4(ELN):c.381G>A (p.Ala127=)	rs148216123	0.00019
NM_000501.4(ELN):c.249C>T (p.Pro83=)	rs565001805	0.00016

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