List of variants in gene RAB7A reported as uncertain significance for Charcot-Marie-Tooth disease

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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
NM_004637.5(RAB7A):c.385C>T (p.Leu129Phe)	rs121909078
NM_004637.5(RAB7A):c.471G>C (p.Lys157Asn)	rs121909081
NM_004637.5(RAB7A):c.482A>C (p.Asn161Thr)	rs121909080
NM_004637.5(RAB7A):c.482A>T (p.Asn161Ile)	rs121909080
NM_004637.5(RAB7A):c.484G>A (p.Val162Met)	rs121909079
NM_004637.6(RAB7A):c.331A>G (p.Ser111Gly)	rs0
NM_004637.6(RAB7A):c.331del (p.Ser111fs)	rs1576303712

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