List of variants reported as uncertain significance for Arthrogryposis, renal dysfunction, and cholestasis 2

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001193315.2(VIPAS39):c.1455C>A (p.Ser485Arg)	rs145453157	0.00129
NM_001193315.2(VIPAS39):c.494G>A (p.Arg165Gln)	rs376797384	0.00001
NM_001193315.2(VIPAS39):c.1003A>G (p.Thr335Ala)	rs867268041
NM_001193315.2(VIPAS39):c.1180-1G>C
NM_001193315.2(VIPAS39):c.1366G>A (p.Asp456Asn)	rs2078466084

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