List of variants in gene combination CCNH, RASA1 reported as benign by GeneDx

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_002890.3(RASA1):c.1017+65G>A	rs3752862	0.60168
NM_002890.3(RASA1):c.2011+237T>C	rs10067098	0.45456
NM_002890.3(RASA1):c.829-193G>A	rs2271235	0.41913
NM_002890.3(RASA1):c.1934+141T>A	rs6898715	0.29191
NM_002890.3(RASA1):c.3060+214A>C	rs72783711	0.15104
NM_002890.3(RASA1):c.2185-155A>G	rs6888938	0.06887
NM_002890.3(RASA1):c.1699-132T>C	rs76905047	0.04056
NM_002890.3(RASA1):c.1777-14T>A	rs36000817	0.03681
NM_002890.3(RASA1):c.693-158A>G	rs74492894	0.03343
NM_002890.3(RASA1):c.693-274_693-273del	rs112878220	0.03342
NM_002890.3(RASA1):c.2691-64T>C	rs12109912	0.02620
NM_002890.3(RASA1):c.1777-16A>T	rs75512926	0.02314
NM_002890.3(RASA1):c.2011+56A>G	rs73156398	0.02269
NM_002890.3(RASA1):c.1049+40A>G	rs113053589	0.01657
NM_002890.3(RASA1):c.1610+29C>T	rs114609431	0.00209
NM_002890.3(RASA1):c.2603+42A>G	rs140502802	0.00121
NM_002890.3(RASA1):c.3061-48T>C	rs377521426	0.00059
NM_002890.3(RASA1):c.1583A>G (p.Tyr528Cys)	rs145752649	0.00043
NM_002890.3(RASA1):c.2766A>T (p.Pro922=)	rs137898246	0.00025
NM_002890.3(RASA1):c.3061-26T>C	rs144049668	0.00008
NM_002890.3(RASA1):c.1049+36dup	rs35694079
NM_002890.3(RASA1):c.1454-7del	rs60835976
NM_002890.3(RASA1):c.1699-69dup	rs35014912
NM_002890.3(RASA1):c.1699-70_1699-69dup	rs35014912
NM_002890.3(RASA1):c.1777-3del	rs377722838
NM_002890.3(RASA1):c.1934+140_1934+141insA	rs375254139
NM_002890.3(RASA1):c.1935-100dup	rs200643915
NM_002890.3(RASA1):c.2184+9_2184+10insGTTAAA	rs863223716
NM_002890.3(RASA1):c.2759-190T>C	rs10942503

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