List of variants reported as likely pathogenic for Arthrogryposis, renal dysfunction, and cholestasis 2

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001193315.2(VIPAS39):c.463_464del (p.Trp155fs)	rs747670551	0.00001
NM_001193315.2(VIPAS39):c.1048-1G>A
NM_001193315.2(VIPAS39):c.1048-1G>T	rs2503151300
NM_001193315.2(VIPAS39):c.157_160del (p.Asp53fs)
NM_001193315.2(VIPAS39):c.166C>T (p.Arg56Ter)
NM_001193315.2(VIPAS39):c.618_626dup (p.Arg206_Leu208dup)	rs1594910243
NM_001193315.2(VIPAS39):c.677A>G (p.His226Arg)	rs1555366438
NM_001193315.2(VIPAS39):c.837-2A>C
NM_001193315.2(VIPAS39):c.958C>T (p.Arg320Ter)	rs747749610

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