List of variants in gene AGBL1 reported as uncertain significance for posterior corneal dystrophy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001386094.1(AGBL1):c.3157C>T (p.Arg1053Trp)	rs185919705	0.00200
NM_001386094.1(AGBL1):c.3044G>C (p.Cys1015Ser)	rs181958589	0.00124
NM_001386094.1(AGBL1):c.985A>T (p.Thr329Ser)	rs745458688	0.00002
NM_001386094.1(AGBL1):c.2674C>T (p.Arg892Ter)
NM_001386094.1(AGBL1):c.785A>C (p.Gln262Pro)
NM_001386094.1(AGBL1):c.968A>G (p.Glu323Gly)

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