Variant (rsID / SNP)

rs34823161

rs34823161 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LARS1. Location: chromosome 5, position 145,503,564. Clinical significance in the table: Benign.

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Reference-table entries

LARS1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:145503564
Cytoband: 5q32
HGVS: NM_020117.11(LARS1):c.3077A>G (p.Tyr1026Cys)
Allele change: Missense_Y999C

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.