"GeneDx"[submitter] AND "REN"[gene] - ClinVar

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Search results

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1049731	NM_000537.4(REN):c.1220G>T (p.Ter407Leu)	REN	Single nucleotide variant (stop lost)	not provided	GUncertain significance
Select item 1177782	NM_000537.4(REN):c.1060-66del	REN	Deletion (intron variant)	not provided	GBenign
Select item 1281982	NM_000537.4(REN):c.1060-240T>C	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239591	NM_000537.4(REN):c.1059+83G>A	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236555	NM_000537.4(REN):c.961-43C>T	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1180062	NM_000537.4(REN):c.960+34G>T	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1284066	NM_000537.4(REN):c.819-45TCTG[10]	REN	Microsatellite (intron variant)	not provided	GBenign
Select item 1263110	NM_000537.4(REN):c.819-45TCTG[9]	REN	Microsatellite (intron variant)	not provided	GBenign
Select item 1288570	NM_000537.4(REN):c.819-45TCTG[6]	REN	Microsatellite (intron variant)	not provided	GBenign
Select item 1283380	NM_000537.4(REN):c.819-62A>C	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247423	NM_000537.4(REN):c.699-63A>G	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281962	NM_000537.4(REN):c.698+111C>T	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295154	NM_000537.4(REN):c.689+254G>A	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249555	NM_000537.4(REN):c.493-131A>C	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226180	NM_000537.4(REN):c.492+134A>G	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 256380	NM_000537.4(REN):c.492+17T>G	REN	Single nucleotide variant (intron variant)	Familial juvenile hyperuricemic nephropathy type 2 +4 more	GBenign
Select item 1272972	NM_000537.4(REN):c.373+293C>A	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267199	NM_000537.4(REN):c.373+196dup	REN	Duplication (intron variant)	not provided	GBenign
Select item 1268413	NM_000537.4(REN):c.373+44C>G	REN	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1223960	NM_000537.4(REN):c.249+110G>A	REN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289859	NM_000537.4(REN):c.249+79_249+80del	REN	Deletion (intron variant)	not provided	GBenign
Select item 1307019	NM_000537.4(REN):c.249+5G>A	REN	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1304113	NM_000537.4(REN):c.230T>G (p.Ile77Ser)	REN (I77S)	Single nucleotide variant (missense variant)	Familial juvenile hyperuricemic nephropathy type 2 +2 more	GUncertain significance
Select item 256379	NM_000537.4(REN):c.204A>C (p.Thr68=)	REN	Single nucleotide variant (synonymous variant)	Familial juvenile hyperuricemic nephropathy type 2 +3 more	GBenign
Select item 253654	GRCh37/hg19 1q31.3-42.13(chr1:197811907-228997888)x3	ACBD3, ADIPOR1 +242 more	Copy number gain	See cases	GPathogenic

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Items: 25