Variant (rsID / SNP)

rs781520666

rs781520666 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GARS1. Location: chromosome 7, position 30,634,540. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GARS1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:30634540
Cytoband: 7p14.3
HGVS: NM_002047.4(GARS1):c.3G>A (p.Met1Ile)
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.