List of variants in gene combination CRPPA, LOC129389757 reported as uncertain significance for Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7; Autosomal recessive limb-girdle muscular dystrophy type 2U

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001101426.4(CRPPA):c.1252-3C>T	rs2128361106
NM_001101426.4(CRPPA):c.1252G>T (p.Asp418Tyr)	rs1781843954
NM_001101426.4(CRPPA):c.1272G>C (p.Glu424Asp)	rs2064970438
NM_001101426.4(CRPPA):c.1275T>A (p.Ser425Arg)	rs1781843424

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