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Variant (rsID / SNP)

rs201818691

PLEC

rs201818691 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEC. Location: chromosome 8, position 145,004,474. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PLECConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
8:145004474
Cytoband
8q24.3
HGVS
NM_201384.3(PLEC):c.2458-8C>T
Allele change
Silent

Associated conditions / phenotypes

Autosomal recessive limb-girdle muscular dystrophy type 2Q|Epidermolysis bullosa simplex 5B, with muscular dystrophy|Epidermolysis bullosa simplex 5C, with pyloric atresia|Epidermolysis bullosa simplex with nail dystrophy|Epidermolysis bullosa simplex, Ogna type

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.