MIR6735[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2672311	Single allele	A3GALT2, ACOT11 +1226 more	Inversion	Bilateral polymicrogyria	GLikely pathogenic
Select item 59966	GRCh38/hg38 1p34.2-34.1(chr1:40462415-44668040)x1	ARTN, ATP6V0B +279 more	Copy number loss	See cases	GPathogenic
Select item 57093	GRCh38/hg38 1p34.2-34.1(chr1:40693289-44514104)x1	ARTN, ATP6V0B +253 more	Copy number loss	See cases	GPathogenic
Select item 3062343	GRCh38/hg38 1p34.2(chr1:42278946-43598390)	C1orf210, C1orf50 +91 more	Copy number loss	Epilepsy syndrome	GPathogenic
Select item 658448	NC_000001.11:g.(?_43446935)_(43450500_?)del	MIR6735, SZT2 +1 more	Deletion	not provided	GUncertain significance
Select item 1634781	NM_001365999.1(SZT2):c.9970-15T>C	MIR6735, SZT2 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 416957	NM_001365999.1(SZT2):c.9970-9C>T	MIR6735, SZT2 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 241040	NM_001365999.1(SZT2):c.9970-7C>G	MIR6735, SZT2 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign

ClinVar