List of variants in gene SLITRK6 reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_032229.3(SLITRK6):c.1524G>A (p.Leu508=)	rs3825413	0.76338
NM_032229.3(SLITRK6):c.1241A>G (p.Gln414Arg)	rs17080147	0.08910
NM_032229.3(SLITRK6):c.222C>T (p.Asn74=)	rs35342386	0.02140
NM_032229.3(SLITRK6):c.327T>C (p.Asn109=)	rs35119660	0.02127
NM_032229.3(SLITRK6):c.73C>T (p.Leu25Phe)	rs12863734	0.01903
NM_032229.3(SLITRK6):c.39T>A (p.Leu13=)	rs74104527	0.00860
NM_032229.3(SLITRK6):c.1920A>G (p.Lys640=)	rs17080144	0.00753
NM_032229.3(SLITRK6):c.592T>C (p.Leu198=)	rs80087848	0.00105
NM_032229.3(SLITRK6):c.1318T>G (p.Leu440Val)	rs200767869	0.00023
NM_032229.3(SLITRK6):c.1656C>A (p.Leu552=)	rs372616753	0.00015
NM_032229.3(SLITRK6):c.1806G>A (p.Thr602=)	rs375333967	0.00009
NM_032229.3(SLITRK6):c.1029T>C (p.Leu343=)	rs200156618	0.00007

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