Variant (rsID / SNP)

rs4303883

rs4303883 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNBP. Location: chromosome 3, position 128,890,350. The table records no clinical significance for this variant.

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Reference-table entries

CNBPNot classified

Variant type: synonymous_variant
Chromosome / position: 3:128890350
HGVS: NM_001127192.2,c.156C>T,p.Asp52Asp
Allele change: Synonymous_D52D

Associated conditions / phenotypes

Myotonic Dystrophy 2|Myotonic Dystrophy 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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