List of variants reported as uncertain significance for Leukodystrophy, hypomyelinating, 16

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001134232.2(TMEM106B):c.167G>T (p.Arg56Ile)	rs1193564382	0.00001
NM_001134232.2(TMEM106B):c.464A>G (p.Asn155Ser)	rs1200294788	0.00001
NM_001134232.2(TMEM106B):c.322C>G (p.Leu108Val)
NM_001134232.2(TMEM106B):c.523G>A (p.Val175Ile)	rs2534923547
NM_001134232.2(TMEM106B):c.55G>C (p.Asp19His)	rs1781655491
NM_001134232.2(TMEM106B):c.697A>G (p.Thr233Ala)	rs2534927399

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