List of variants in gene RIT1 reported as pathogenic by Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_006912.6(RIT1):c.170C>G (p.Ala57Gly)	rs672601334
NM_006912.6(RIT1):c.229G>A (p.Ala77Thr)	rs869025191
NM_006912.6(RIT1):c.245T>C (p.Phe82Ser)	rs868208063
NM_006912.6(RIT1):c.246T>A (p.Phe82Leu)	rs730881014
NM_006912.6(RIT1):c.247A>C (p.Thr83Pro)	rs869025195
NM_006912.6(RIT1):c.69A>C (p.Lys23Asn)	rs1557962794
NM_006912.6(RIT1):c.91G>C (p.Gly31Arg)	rs1571999498

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