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Variant (rsID / SNP)

rs2256135

SYNE1

rs2256135 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYNE1. Location: chromosome 6, position 152,464,839. Clinical significance in the table: Benign.

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Reference-table entries

SYNE1Benign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
6:152464839
Cytoband
6q25.2
HGVS
NM_182961.4(SYNE1):c.25038T>C (p.Arg8346=)
Allele change
Synonymous_R548R

Associated conditions / phenotypes

Autosomal recessive ataxia, Beauce type|Emery-Dreifuss muscular dystrophy 4, autosomal dominant|Emery-Dreifuss muscular dystrophy 4, autosomal dominant|Autosomal recessive ataxia, Beauce type|Arthrogryposis multiplex congenita 3, myogenic type

Public references

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