List of variants in gene TLL2 reported as uncertain significance for anterior horn disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_012465.4(TLL2):c.112G>C (p.Glu38Gln)	rs1292893658
NM_012465.4(TLL2):c.1609C>T (p.His537Tyr)	rs1589410819

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