List of variants reported as uncertain significance for KINSSHIP syndrome

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001386135.1(AFF3):c.1108C>T (p.Leu370Phe)	rs1232476839	0.00001
NM_001386135.1(AFF3):c.127G>C (p.Asp43His)
NM_001386135.1(AFF3):c.1518C>A (p.Asp506Glu)	rs2546110903
NM_001386135.1(AFF3):c.1678G>T (p.Ala560Ser)
NM_001386135.1(AFF3):c.1823CCGCGG[3] (p.Ala611_Asp612insAlaAla)	rs1558618319
NM_001386135.1(AFF3):c.53+41939G>A	rs1687368963
NM_001386135.1(AFF3):c.664T>A (p.Ser222Thr)	rs2469091128
NM_001386135.1(AFF3):c.736G>C (p.Asp246His)	rs2469090114
NM_001386135.1:c.-64-274CGG[(797_850)]

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