Variant (rsID / SNP)

rs114286107

rs114286107 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGXT2. Location: chromosome 5, position 35,013,058. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

AGXT2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:35013058
Cytoband: 5p13.2
HGVS: NM_031900.4(AGXT2):c.1188+1G>A
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.