Variant (rsID / SNP)

rs118002895

rs118002895 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GARS1. Location: chromosome 7, position 30,668,131. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GARS1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:30668131
Cytoband: 7p14.3
HGVS: NM_002047.4(GARS1):c.1700-45T>C
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.