List of variants in gene combination CRPPA, LOC129998004 reported as likely benign for Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7; Autosomal recessive limb-girdle muscular dystrophy type 2U

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001101426.4(CRPPA):c.171G>A (p.Gly57=)	rs1032859096	0.00002
NM_001101426.4(CRPPA):c.189C>T (p.Pro63=)	rs1788325301	0.00001
NM_001101426.4(CRPPA):c.138C>G (p.Ala46=)	rs1162623078
NM_001101426.4(CRPPA):c.159C>A (p.Ala53=)

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