Variants in gene ASS1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_054012.4(ASS1):c.501C>T (p.His167=)	rs10901072	0.12154
NM_054012.4(ASS1):c.766G>A (p.Glu256Lys)	rs74923032	0.00937
NM_054012.4(ASS1):c.364-6T>C	rs116103138	0.00881
NM_054012.4(ASS1):c.675C>T (p.Ile225=)	rs58233547	0.00735
NM_054012.4(ASS1):c.106-10T>G	rs73541957	0.00593
NM_054012.4(ASS1):c.622A>G (p.Thr208Ala)	rs62637575	0.00277
NM_054012.4(ASS1):c.421-28C>T	rs76169404	0.00175
NM_054012.4(ASS1):c.363+16A>G	rs191432165	0.00099
NM_054012.4(ASS1):c.323G>T (p.Arg108Leu)	rs35269064

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