Variant (rsID / SNP)

rs199728745

rs199728745 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RARS2. Location: chromosome 6, position 88,229,382. Clinical significance in the table: Pathogenic.

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Reference-table entries

RARS2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 6:88229382
Cytoband: 6q15
HGVS: NM_020320.5(RARS2):c.1156C>T (p.Arg386Ter)
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.