List of variants in gene combination ASS1, LOC130002809 reported as uncertain significance for inborn disorder of amino acid metabolism

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_054012.3(ASS1):c.-171G>A	rs886063529	0.00063
NM_054012.3(ASS1):c.-146_-145dup	rs886063530
NM_054012.3(ASS1):c.-185A>G	rs886063528
NM_054012.3(ASS1):c.-203C>G	rs886063527
NM_054012.3(ASS1):c.-217G>T	rs1427339813
NM_054012.3(ASS1):c.-233G>C	rs886063526
NM_054012.3(ASS1):c.-233G>T	rs886063526

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