From: Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)
 | rs-number/Polymorphism |
---|---|
SPG31 intron 1 | rs1863059 |
SPG31 intron 2 | rs1863058 |
 | rs1863056 |
SPG31 exon 4 | rs2276625 |
SPG31 intron 5 | rs12988844 |
SPG31 intron 6 | c.595-19T>G, G allele: 1,2% |
SPG31 3'UTR | c.606+155T>C, C allele: 1,2% |