List of variants reported as uncertain significance for Renal tubular dysgenesis of genetic origin by Department of Pathology and Laboratory Medicine, Sinai Health System

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NC_000001.11:g.230704288G>T	rs1805090	0.00134
NM_000789.4(ACE):c.1979C>G (p.Ser660Cys)	rs147429960	0.00098
NM_000789.4(ACE):c.863A>G (p.Gln288Arg)	rs199591851	0.00064
NM_000789.4(ACE):c.1444C>T (p.Arg482Cys)	rs201540553	0.00028
NM_000789.4(ACE):c.1459C>T (p.Arg487Cys)	rs149784122	0.00019
NM_001384479.1(AGT):c.862C>T	rs61762530	0.00013
NM_001384479.1(AGT):c.-24C>T	rs764314612	0.00009
NM_001384479.1(AGT):c.382A>G (p.Thr128Ala)	rs138340265	0.00007
NM_000685.5(AGTR1):c.113T>C (p.Ile38Thr)	rs751575775	0.00001
NM_000789.4(ACE):c.1852G>A (p.Gly618Ser)
NM_000789.4(ACE):c.2570G>A (p.Arg857His)	rs146089353
NM_000789.4(ACE):c.3533C>T (p.Pro1178Leu)
NM_001384479.1(AGT):c.1096C>T (p.Arg366Trp)
NM_001384479.1(AGT):c.1180_1182dup (p.Ala394dup)	rs562507867
NM_001384479.1(AGT):c.1361C>T (p.Ala454Val)

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