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

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Search results

Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1271638	NM_003162.4(STRN):c.*101T>G	STRN	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1275078	NM_003162.4(STRN):c.*5A>G	STRN	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1249083	NM_003162.4(STRN):c.2087-72G>T	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1241402	NM_003162.4(STRN):c.2087-233C>T	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245944	NM_003162.4(STRN):c.2086+36_2086+37dup	STRN	Duplication (intron variant)	not provided	GBenign
Select item 1229283	NM_003162.4(STRN):c.2086+36dup	STRN	Duplication (intron variant)	not provided	GBenign
Select item 1262898	NM_003162.4(STRN):c.1979-104C>T	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249012	NM_003162.4(STRN):c.1979-138C>T	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258328	NM_003162.4(STRN):c.1978+321C>T	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249221	NM_003162.4(STRN):c.1978+111_1978+112del	STRN	Deletion (intron variant)	not provided	GBenign
Select item 1237891	NM_003162.4(STRN):c.1838-200G>A	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282192	NM_003162.4(STRN):c.1837+282A>G	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265233	NM_003162.4(STRN):c.1670-308C>T	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279384	NM_003162.4(STRN):c.1669+335T>C	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233218	NM_003162.4(STRN):c.1669+192G>A	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231795	NM_003162.4(STRN):c.1547+153G>A	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239451	NM_003162.4(STRN):c.1547+12T>C	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272813	NM_003162.4(STRN):c.1500-135C>G	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271620	NM_003162.4(STRN):c.1500-202A>G	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221199	NM_003162.4(STRN):c.1324-98G>A	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179729	NM_003162.4(STRN):c.1324-137A>G	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274093	NM_003162.4(STRN):c.1187-8C>T	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248225	NM_003162.4(STRN):c.1186+30A>T	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263170	NM_003162.4(STRN):c.932-260GT[16]	STRN	Microsatellite (intron variant)	not provided	GBenign
Select item 1245088	NM_003162.4(STRN):c.932-260GT[15]	STRN	Microsatellite (intron variant)	not provided	GBenign
Select item 1249505	NM_003162.4(STRN):c.795+15T>G	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178368	NM_003162.4(STRN):c.659+108_659+109insTTAA	STRN	Insertion (intron variant)	not provided	GBenign
Select item 1231587	NM_003162.4(STRN):c.412+81T>C	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1298262	NM_003162.4(STRN):c.338+110C>T	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261275	NM_003162.4(STRN):c.235-21T>G	STRN	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222083	NM_003162.4(STRN):c.235-74A>G	STRN	Single nucleotide variant (intron variant)	not provided	GBenign

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Items: 31