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Variant (rsID / SNP)

rs8142483

LARGE1

rs8142483 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LARGE1. Location: chromosome 22, position 34,000,484. Clinical significance in the table: Benign.

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Reference-table entries

LARGE1Benign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
22:34000484
Cytoband
22q12.3
HGVS
NM_133642.5(LARGE1):c.552G>A (p.Thr184=)
Allele change
Synonymous_T184T

Associated conditions / phenotypes

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6|Muscular dystrophy-dystroglycanopathy type B6

Public references

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