List of variants in gene LTBP2 reported as likely pathogenic by Invitae

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000428.3(LTBP2):c.2908+1G>A	rs201872469	0.00019
NM_000428.3(LTBP2):c.2659+2T>C	rs756727211	0.00001
NM_000428.3(LTBP2):c.3151+1G>T	rs1173459626	0.00001
NC_000014.8:g.(?_74976755)_(74988684_?)del
NM_000428.3(LTBP2):c.2369-2A>G
NM_000428.3(LTBP2):c.2389-2A>G	rs1327636983
NM_000428.3(LTBP2):c.2789-1G>A
NM_000428.3(LTBP2):c.3527-1G>C	rs778560568
NM_000428.3(LTBP2):c.3652+1G>C	rs773910322
NM_000428.3(LTBP2):c.4370-2A>C	rs2139689656
NM_000428.3(LTBP2):c.494+1G>T	rs2139815316

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