List of variants reported as likely pathogenic for syndromic intellectual disability by Clinical Genetics and Genomics, Karolinska University Hospital

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_013275.6(ANKRD11):c.3651dup (p.Lys1218fs)
NM_020987.5(ANK3):c.2902G>C (p.Asp968His)	rs730882195
NM_138576.4(BCL11B):c.908del (p.Pro303fs)
NM_203475.3(PORCN):c.887G>C (p.Arg296Pro)

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