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

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_002890.3(RASA1):c.1777-14T>A	rs36000817	0.03681
NM_002890.3(RASA1):c.1777-16A>T	rs75512926	0.02314
NM_002890.3(RASA1):c.1777-15_1777-14insA	rs202147617	0.00998
NM_002890.3(RASA1):c.829-12T>A	rs187379673	0.00276
NM_002890.3(RASA1):c.1102+10T>C	rs150779406	0.00268
NM_002890.3(RASA1):c.2691-11C>T	rs149730288	0.00264
NM_002890.3(RASA1):c.1371G>A (p.Lys457=)	rs140707293	0.00208
NM_002890.3(RASA1):c.2528C>A (p.Thr843Asn)	rs184201084	0.00096
NM_002890.3(RASA1):c.1394G>A (p.Arg465His)	rs181630831	0.00071
NM_002890.3(RASA1):c.1103-17C>T	rs200562377	0.00066
NM_002890.3(RASA1):c.1583A>G (p.Tyr528Cys)	rs145752649	0.00043
NM_002890.3(RASA1):c.2286C>T (p.His762=)	rs373059169	0.00030
NM_002890.3(RASA1):c.1332+8T>C	rs376637789	0.00012
NM_002890.3(RASA1):c.1494G>A (p.Glu498=)	rs200197533	0.00009
NM_002890.3(RASA1):c.1968A>T (p.Ile656=)	rs370819852	0.00006
NM_002890.3(RASA1):c.2259C>T (p.Ala753=)	rs552498036	0.00005
NM_002890.3(RASA1):c.3067T>C (p.Leu1023=)	rs3747704	0.00003
NM_002890.3(RASA1):c.2288A>T (p.Glu763Val)	rs373098580	0.00002
NM_002890.3(RASA1):c.1333-10dup	rs775819060
NM_002890.3(RASA1):c.1454-7del	rs60835976
NM_002890.3(RASA1):c.1454-7dup	rs60835976
NM_002890.3(RASA1):c.1454-9_1454-7del
NM_002890.3(RASA1):c.1777-3del	rs377722838
NM_002890.3(RASA1):c.1777-3dup	rs377722838
NM_002890.3(RASA1):c.2488-3del
NM_002890.3(RASA1):c.612T>C (p.Tyr204=)	rs377014568
NM_002890.3(RASA1):c.693-14dup	rs776195697

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