List of variants in gene SUMO1 reported as uncertain significance for orofacial cleft

Minimum submission review status:		Collection method:
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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_003352.8(SUMO1):c.*776A>T	rs72923015	0.00156
NM_003352.8(SUMO1):c.*884A>G	rs555380378	0.00070
NM_003352.8(SUMO1):c.*944G>C	rs537401465	0.00028
NM_003352.8(SUMO1):c.*475A>G	rs754482827	0.00020
NM_003352.8(SUMO1):c.-83A>G	rs535659845	0.00004
NM_003352.8(SUMO1):c.88-8C>T	rs778978037	0.00004
NM_003352.8(SUMO1):c.*545G>T	rs747664973	0.00003
NM_003352.8(SUMO1):c.*724A>G	rs886055457	0.00001
NM_003352.8(SUMO1):c.*814G>A	rs753364030	0.00001
NM_003352.8(SUMO1):c.*1038C>T	rs1692651255
NM_003352.8(SUMO1):c.*753C>G	rs1035640561
NM_003352.8(SUMO1):c.-48C>T	rs976294034

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