List of variants in gene LRSAM1 reported as uncertain significance for Charcot-Marie-Tooth disease type 2

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001005373.4(LRSAM1):c.1860C>T (p.His620=)	rs147734401	0.00054
NM_001005373.4(LRSAM1):c.804C>T (p.Leu268=)	rs771510127	0.00003
NM_001005373.4(LRSAM1):c.1011C>T (p.Ser337=)	rs886063456	0.00001
NM_001005373.4(LRSAM1):c.-189+120_-189+122del	rs749626964

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