List of variants in gene combination CCNH, RASA1 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 8

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HGVS	dbSNP	gnomAD frequency
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.1583A>G (p.Tyr528Cys)	rs145752649	0.00043
NM_002890.3(RASA1):c.1332+8T>C	rs376637789	0.00012
NM_002890.3(RASA1):c.3132T>C (p.Asn1044=)	rs149297860	0.00006
NM_002890.3(RASA1):c.1454-7del	rs60835976
NM_002890.3(RASA1):c.2691-17del	rs368117332
NM_002890.3(RASA1):c.829-12del	rs564571974

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