Variant (rsID / SNP)

rs141539149

rs141539149 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KARS1. Location: chromosome 16, position 75,669,867. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

KARS1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:75669867
Cytoband: 16q23.1
HGVS: NM_005548.3(KARS1):c.612A>G (p.Thr204=)
Allele change: Synonymous_T232T

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.