ClinVar Miner

List of variants in gene RINT1 reported as likely pathogenic for papillary adenocarcinoma

Included ClinVar conditions (8):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_021930.6(RINT1):c.1107+1G>T	rs200989342	0.00001
NM_021930.6(RINT1):c.1021C>G (p.Leu341Val)	rs151055286

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