ClinVar Miner

List of variants reported as pathogenic for papillary renal cell carcinoma by Mendelics

Included ClinVar conditions (4):

Hereditary papillary renal cell carcinoma
Osteofibrous dysplasia; Papillary renal cell carcinoma type 1; Hepatocellular carcinoma; Autosomal recessive nonsyndromic hearing loss 97
Papillary renal cell carcinoma type 1
Von Hippel-Lindau syndrome; Cerebellar hemangioblastoma; Papillary renal cell carcinoma type 1; Skin adenoma

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004958.4(MTOR):c.3026G>A (p.Arg1009Gln)	rs778855567	0.00003
NM_000245.4(MET):c.3274G>A (p.Val1092Ile)	rs786202724	0.00001

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