List of variants reported as uncertain significance for autosomal recessive non-syndromic intellectual disability by Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_138775.3(ALKBH8):c.844A>T (p.Met282Leu)	rs763543231	0.00001
NM_138775.3(ALKBH8):c.1442G>A (p.Arg481His)	rs532327456

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