List of variants reported as pathogenic for Arterial calcification, generalized, of infancy, 2 by OMIM

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001171.6(ABCC6):c.3421C>T (p.Arg1141Ter)	rs72653706	0.00122
NM_001171.6(ABCC6):c.3940C>T (p.Arg1314Trp)	rs63750759	0.00069
NM_001171.6(ABCC6):c.2787+1G>T	rs72664209	0.00017
NM_001171.6(ABCC6):c.2294G>A (p.Arg765Gln)	rs67561842	0.00006
NM_001171.6(ABCC6):c.1552C>T (p.Arg518Ter)	rs72650700	0.00004
NM_001171.6(ABCC6):c.3736-1G>A	rs63750273	0.00001
NM_001171.6(ABCC6):c.4216C>A (p.Gln1406Lys)	rs387906859
NM_001171.6(ABCC6):c.450dup (p.Ala151fs)	rs387906860

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