Variant (rsID / SNP)

rs146490489

rs146490489 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FUS. Location: chromosome 16, position 31,204,751. Clinical significance in the table: Likely benign.

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Reference-table entries

FUSLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:31204751
Cytoband: 16p11.2
HGVS: NM_004960.3(FUS):c.*1992A>C
Allele change: Silent

Associated conditions / phenotypes

Amyotrophic lateral sclerosis type 6

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.