List of variants in gene RINT1 reported as uncertain significance for Hereditary breast ovarian cancer syndrome

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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_021930.6(RINT1):c.448A>C (p.Ser150Arg)	rs780699445	0.00003
NM_021930.6(RINT1):c.814T>C (p.Cys272Arg)	rs761066440	0.00003
NM_021930.6(RINT1):c.1246C>T (p.His416Tyr)	rs1221027048
NM_021930.6(RINT1):c.202C>T (p.Leu68Phe)	rs1790249927
NM_021930.6(RINT1):c.311G>A (p.Arg104Gln)	rs866948739

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