Variant (rsID / SNP)

rs116930926

rs116930926 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NARS2. Location: chromosome 11, position 78,189,653. Clinical significance in the table: Benign.

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Reference-table entries

NARS2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:78189653
Cytoband: 11q14.1
HGVS: NM_024678.6(NARS2):c.899A>G (p.Lys300Arg)
Allele change: Missense_K73R

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.