List of variants in gene RIT1 reported as uncertain significance for RIT1-related disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_006912.6(RIT1):c.38G>A (p.Ser13Asn)	rs145034964	0.00012
NM_006912.6(RIT1):c.23T>C (p.Val8Ala)	rs977203137
NM_006912.6(RIT1):c.375C>A (p.Asp125Glu)	rs34831194
NM_006912.6(RIT1):c.488C>T (p.Thr163Ile)	rs2102581107
NM_006912.6(RIT1):c.550A>G (p.Arg184Gly)	rs1453467370

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