List of variants reported as pathogenic for myopia 27 by OMIM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_013291.3(CPSF1):c.2823_2824del (p.Val943fs)	rs782640869	0.00009
NM_013291.3(CPSF1):c.1858C>T (p.Gln620Ter)	rs1586620121
NM_013291.3(CPSF1):c.3823G>T (p.Asp1275Tyr)	rs1554862601
NM_013291.3(CPSF1):c.4146-2A>G	rs782555528

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