Variant (rsID / SNP)

rs3219174

rs3219174 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALS2. Location: chromosome 2, position 202,565,681. Clinical significance in the table: Benign.

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Reference-table entries

ALS2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:202565681
Cytoband: 2q33.1
HGVS: NM_020919.4(ALS2):c.*893C>T
Allele change: Silent

Associated conditions / phenotypes

Amyotrophic lateral sclerosis type 2, juvenile|ALS2-Related Disorders

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.