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Variant (rsID / SNP)

rs142067801

YARS2

rs142067801 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to YARS2. Location: chromosome 12, position 32,906,929. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

YARS2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
12:32906929
Cytoband
12p11.21
HGVS
NM_001040436.3(YARS2):c.870T>C (p.Val290=)
Allele change
Synonymous_V290V

Associated conditions / phenotypes

Myopathy, lactic acidosis, and sideroblastic anemia 2|Myopathy, lactic acidosis, and sideroblastic anemia

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.