NM_000023.4(SGCA):c.157+20C>A AND Autosomal recessive limb-girdle muscular dystrophy type 2D
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 9, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003039062.3
Allele description [Variation Report for NM_000023.4(SGCA):c.157+20C>A]
NM_000023.4(SGCA):c.157+20C>A
Condition(s)
- Name:
- Autosomal recessive limb-girdle muscular dystrophy type 2D (LGMDR3)
- Synonyms:
- ADHALINOPATHY, PRIMARY; Limb-girdle muscular dystrophy, type 2D; Muscular dystrophy limb-girdle with alpha-sarcoglycan; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0011968; MedGen: C2936332; Orphanet: 62; OMIM: 608099
-
solute carrier family 22 member 4 [Danio rerio]
solute carrier family 22 member 4 [Danio rerio]gi|41053589|ref|NP_957143.1|Protein
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Last Updated: Sep 29, 2024