List of variants in gene combination LOC106736614, RET reported as uncertain significance for renal hypodysplasia/aplasia 1

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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_020975.6(RET):c.-132G>T	rs886046985	0.00103
NM_020975.6(RET):c.-51C>T	rs765384640	0.00012
NM_020975.6(RET):c.-158G>A	rs886046984	0.00001
NM_020975.6(RET):c.-173A>G	rs1359755826
NM_020975.6(RET):c.-187C>A	rs886046983

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