List of variants in gene ASS1 reported as likely benign for not provided

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_054012.4(ASS1):c.970+69C>T	rs78879495	0.01405
NM_054012.4(ASS1):c.838+92C>T	rs116522126	0.01256
NM_054012.4(ASS1):c.-6+44G>C	rs151254686	0.01252
NM_054012.4(ASS1):c.970+208C>A	rs116301216	0.01213
NM_054012.4(ASS1):c.105+290C>T	rs149558736	0.01085
NM_054012.4(ASS1):c.766G>A (p.Glu256Lys)	rs74923032	0.00937
NM_054012.4(ASS1):c.105+246C>T	rs115788113	0.00743
NM_054012.4(ASS1):c.106-10T>G	rs73541957	0.00593
NM_054012.4(ASS1):c.-5-93C>T	rs75950322	0.00538
NM_054012.4(ASS1):c.971-144C>T	rs114867341	0.00473
NM_054012.4(ASS1):c.-5-1904G>A	rs184403245	0.00399
NM_054012.4(ASS1):c.566+172A>G	rs149311811	0.00363
NM_054012.4(ASS1):c.364-136C>T	rs58429097	0.00354
NM_054012.4(ASS1):c.-5-41C>T	rs73541954	0.00350
NM_054012.4(ASS1):c.838+118C>T	rs60444687	0.00292
NM_054012.4(ASS1):c.622A>G (p.Thr208Ala)	rs62637575	0.00277
NM_054012.4(ASS1):c.567-22G>C	rs147147298	0.00255
NM_054012.4(ASS1):c.421-28C>T	rs76169404	0.00175
NM_054012.4(ASS1):c.1101G>A (p.Leu367=)	rs139031154	0.00128
NM_054012.4(ASS1):c.420+13T>G	rs201883474	0.00099
NM_054012.4(ASS1):c.333C>T (p.Ala111=)	rs141568959	0.00031
NM_054012.4(ASS1):c.489C>T (p.Tyr163=)	rs377319610	0.00012
NM_054012.4(ASS1):c.323G>T (p.Arg108Leu)	rs35269064
NM_054012.4(ASS1):c.510C>A (p.Pro170=)
NM_054012.4(ASS1):c.566+18C>G	rs200036163
NM_054012.4(ASS1):c.597+167C>A	rs28633982
NM_054012.4(ASS1):c.597+206C>T	rs184410370
NM_054012.4(ASS1):c.773+23G>T	rs146390729
NM_054012.4(ASS1):c.774-28G>T	rs151042066
NM_054012.4(ASS1):c.957G>A (p.Glu319=)	rs1588503739

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