List of variants reported as likely benign for syndromic intellectual disability by Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001184880.2(PCDH19):c.2873G>A (p.Arg958Gln)	rs748581653	0.00006
NM_152564.5(VPS13B):c.2885C>T (p.Thr962Met)	rs547184348	0.00003
NM_001353921.2(ARHGEF9):c.1497T>G (p.Phe499Leu)	rs2147114173

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