Variant (rsID / SNP)

rs2799064

rs2799064 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGRN. Location: chromosome 1, position 957,898. Clinical significance in the table: Benign.

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Reference-table entries

AGRNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:957898
Cytoband: 1p36.33
HGVS: NM_198576.4(AGRN):c.463+56G>T
Allele change: Silent

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.