"GeneDx"[submitter] AND "WNT3"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1296567	NM_030753.5(WNT3):c.*8+232T>C	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1318109	NM_030753.5(WNT3):c.*8+140G>A	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1318001	NM_030753.5(WNT3):c.589-210G>A	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1242139	NM_030753.5(WNT3):c.323-252C>G	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237348	NM_030753.5(WNT3):c.323-293G>C	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290887	NM_030753.5(WNT3):c.322+38T>G	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1318339	NM_030753.5(WNT3):c.322+33_322+34del	LRRC37A2, WNT3	Deletion (intron variant)	not provided	GLikely benign
Select item 1317816	NM_030753.5(WNT3):c.322+34T>G	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1318201	NM_030753.5(WNT3):c.322+33C>G	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1259133	NM_030753.5(WNT3):c.322+19dup	LRRC37A2, WNT3	Duplication (intron variant)	not provided	GBenign
Select item 1253429	NM_030753.5(WNT3):c.322+28A>G	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290338	NM_030753.5(WNT3):c.322+18A>G	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 515621	NM_030753.5(WNT3):c.322+18del	LRRC37A2, WNT3	Deletion (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 1320553	NM_030753.5(WNT3):c.322+16T>G	WNT3, LRRC37A2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1318034	NM_030753.5(WNT3):c.322+15C>G	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316273	NM_030753.5(WNT3):c.81-194dup	LOC111589213, LRRC37A2 +1 more	Duplication (intron variant)	not provided	GLikely benign
Select item 1318404	NM_030753.5(WNT3):c.80+72G>C	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1317620	NM_030753.5(WNT3):c.80+53G>T	LRRC37A2, WNT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1316274	NC_000017.11:g.46819041C>A	LRRC37A2, WNT3	Single nucleotide variant	not provided	GLikely benign
Select item 1317834	NC_000017.11:g.46819047G>T	LRRC37A2, WNT3	Single nucleotide variant	not provided	GLikely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 20