Variant (rsID / SNP)

rs181665720

rs181665720 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LARS2. Location: chromosome 3, position 45,537,908. Clinical significance in the table: Benign.

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Reference-table entries

LARS2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:45537908
Cytoband: 3p21.31
HGVS: NM_015340.4(LARS2):c.1622+43G>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.