List of variants in gene combination LOC107548112, REN reported as uncertain significance for renal tubular dysgenesis

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000537.4(REN):c.97C>T (p.Arg33Trp)	rs11571098	0.00031
NM_000537.4(REN):c.45G>A (p.Leu15=)	rs142739309	0.00009
NM_000537.4(REN):c.-26A>G	rs1419061434	0.00001
NM_000537.4(REN):c.17G>A (p.Arg6Lys)
NM_000537.4(REN):c.25C>T (p.Arg9Cys)
NM_000537.4(REN):c.26G>A (p.Arg9His)
NM_000537.4(REN):c.35T>C (p.Leu12Pro)
NM_000537.4(REN):c.95A>C (p.Lys32Thr)
NM_000537.4(REN):c.98+18C>T
NM_000537.4(REN):c.98G>A (p.Arg33Gln)

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