List of variants in gene SCLT1 reported as likely pathogenic for not provided

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_144643.4(SCLT1):c.102+2del	rs2125774645
NM_144643.4(SCLT1):c.1146+2_1146+5del
NM_144643.4(SCLT1):c.1147-1G>T
NM_144643.4(SCLT1):c.1218+2T>A	rs2126003617
NM_144643.4(SCLT1):c.1219-1G>A
NM_144643.4(SCLT1):c.1439+1G>A
NM_144643.4(SCLT1):c.1830-2A>G
NM_144643.4(SCLT1):c.1908+1G>T
NM_144643.4(SCLT1):c.425_426+2del
NM_144643.4(SCLT1):c.616-1G>T	rs2126069391
NM_144643.4(SCLT1):c.686_686+3del	rs2126069168
NM_144643.4(SCLT1):c.778-2A>T
NM_144643.4(SCLT1):c.869+1G>T

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