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Variant (rsID / SNP)

rs1056899

SETX

rs1056899 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SETX. Location: chromosome 9, position 135,139,901. Clinical significance in the table: Benign.

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Reference-table entries

SETXBenign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
9:135139901
Cytoband
9q34.13
HGVS
NM_015046.7(SETX):c.7759A>G (p.Ile2587Val)
Allele change
Missense_I2616V

Associated conditions / phenotypes

Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2|Amyotrophic lateral sclerosis type 4|Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2|Amyotrophic lateral sclerosis type 4

Public references

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