ClinVar Miner

List of variants reported as uncertain significance for Charcot-Marie-Tooth disease axonal type 2P by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (1):

Charcot-Marie-Tooth disease axonal type 2P

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001005373.4(LRSAM1):c.1199G>A (p.Arg400Gln)	rs150344223	0.00014
NM_001005373.4(LRSAM1):c.2036T>C (p.Leu679Pro)	rs1564286814

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