List of variants in gene combination INF2, LOC130056630 reported as likely benign for Focal segmental glomerulosclerosis 5; Charcot-Marie-Tooth disease dominant intermediate E

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_022489.4(INF2):c.1949+18C>T	rs1484348980	0.00003
NM_022489.4(INF2):c.1949+10G>A	rs1342614480
NM_022489.4(INF2):c.1949+7G>A	rs757853615

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