ClinVar Miner

List of variants in gene RET studied for Congenital anomaly of kidney and urinary tract

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.1201A>T (p.Ser401Cys)	rs140638866	0.00003
NM_020975.6(RET):c.334C>T (p.Arg112Cys)	rs762626209	0.00001
NM_020975.6(RET):c.1934_1936del (p.Ser645del)	rs1416677590

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