List of variants in gene SLITRK6 reported as pathogenic

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_032229.3(SLITRK6):c.1240C>T (p.Gln414Ter)	rs587777069	0.00016
NM_032229.3(SLITRK6):c.541C>T (p.Arg181Ter)	rs587777071	0.00001
GRCh37/hg19 13q31.1(chr13:85812936-86436723)x1
NM_032229.3(SLITRK6):c.1171del (p.Met391fs)
NM_032229.3(SLITRK6):c.3G>C (p.Met1Ile)	rs2501107669
NM_032229.3(SLITRK6):c.406G>T (p.Glu136Ter)	rs1874712158
NM_032229.3(SLITRK6):c.890C>A (p.Ser297Ter)	rs587777070

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