List of variants in gene RIT1 reported by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006912.6(RIT1):c.116T>G (p.Met39Arg)	rs2102590945
NM_006912.6(RIT1):c.246T>G (p.Phe82Leu)	rs730881014
NM_006912.6(RIT1):c.268A>G (p.Met90Val)	rs1557960039
NM_006912.6(RIT1):c.270G>A (p.Met90Ile)	rs483352822
NM_006912.6(RIT1):c.270G>C (p.Met90Ile)	rs483352822
NM_006912.6(RIT1):c.284G>C (p.Gly95Ala)	rs672601335
NM_006912.6(RIT1):c.551G>C (p.Arg184Thr)	rs1401658925
NM_006912.6(RIT1):c.69A>C (p.Lys23Asn)	rs1557962794

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