List of variants in gene RET reported as benign for renal hypodysplasia/aplasia 1

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.*1506G>A	rs2742241	0.83094
NM_020975.6(RET):c.1296A>G (p.Ala432=)	rs1800860	0.74268
NM_020975.6(RET):c.*1116T>C	rs2435355	0.22170
NM_020975.6(RET):c.2712C>G (p.Ser904=)	rs1800863	0.17043
NM_020975.6(RET):c.*388G>A	rs3026782	0.17032
NM_020975.6(RET):c.*95C>T	rs17028	0.16697
NM_020975.6(RET):c.*1591G>A	rs76759170	0.03751
NM_020975.6(RET):c.3112A>G (p.Thr1038Ala)	rs201740483	0.00047

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