List of variants reported as likely benign for congenital entropion by 3billion, Medical Genetics

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_018993.4(RIN2):c.41G>A (p.Arg14Gln)	rs367797077	0.00032
NM_000052.7(ATP7A):c.1286A>G (p.Glu429Gly)	rs2077660217	0.00001
NM_001042545.2(LTBP4):c.517G>T (p.Val173Leu)	rs755035387	0.00001
NM_000052.7(ATP7A):c.1126A>G (p.Thr376Ala)	rs782616685
NM_000052.7(ATP7A):c.1127C>A (p.Thr376Lys)	rs2077659011
NM_000052.7(ATP7A):c.1835T>G (p.Ile612Ser)	rs1569549840
NM_000052.7(ATP7A):c.278C>G (p.Thr93Arg)	rs539177302
NM_000052.7(ATP7A):c.3103G>A (p.Ala1035Thr)	rs2077968562
NM_000052.7(ATP7A):c.641T>C (p.Val214Ala)
NM_000052.7(ATP7A):c.924A>G (p.Ile308Met)
NM_001042545.2(LTBP4):c.4628C>T (p.Pro1543Leu)
NM_012463.4(ATP6V0A2):c.976G>T (p.Ala326Ser)
NM_018993.4(RIN2):c.28G>A (p.Gly10Ser)	rs535994976
NM_018993.4(RIN2):c.695C>T (p.Ser232Phe)

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