Variant (rsID / SNP)

rs111818381

rs111818381 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGRN. Location: chromosome 1, position 984,971. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

AGRNBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:984971
Cytoband: 1p36.33
HGVS: NM_198576.4(AGRN):c.4540G>A (p.Ala1514Thr)
Allele change: Missense_A1514T

Associated conditions / phenotypes

Congenital myasthenic syndrome 8

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.