List of variants reported as uncertain significance for Arterial calcification, generalized, of infancy, 2

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001171.6(ABCC6):c.1171A>G (p.Arg391Gly)	rs72653762	0.00459
NM_001171.6(ABCC6):c.1108A>G (p.Asn370Asp)	rs72653760	0.00030
NM_001171.6(ABCC6):c.469G>A (p.Gly157Arg)	rs1209940471	0.00003
NM_001171.6(ABCC6):c.1214C>T (p.Ala405Val)	rs115663615
NM_001171.6(ABCC6):c.1853G>A (p.Ser618Asn)
NM_001171.6(ABCC6):c.3952G>A (p.Ala1318Thr)	rs2046496590
NM_001171.6(ABCC6):c.4151T>C (p.Val1384Ala)

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