List of variants in gene combination LOC126862187, RASGRF1 reported as likely benign

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001145648.3(RASGRF1):c.2401G>A (p.Asp801Asn)	rs113161554	0.00158
NM_001145648.3(RASGRF1):c.2148C>T (p.Arg716=)	rs144984287	0.00026
NM_001145648.3(RASGRF1):c.2124C>T (p.Tyr708=)	rs770172047	0.00004
NM_001145648.3(RASGRF1):c.2142C>T (p.Ser714=)

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