List of variants in gene MIP reported as likely pathogenic for cataract

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_012064.4(MIP):c.493_494insT (p.Gly165fs)
NM_012064.4(MIP):c.525+1G>A	rs1868687508
NM_012064.4(MIP):c.559del (p.Arg187fs)

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