Variant (rsID / SNP)

rs2236681

rs2236681 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HYLS1, PUS3. Location: chromosome 11, position 125,770,425. Clinical significance in the table: Benign.

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Reference-table entries

HYLS1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:125770425
Cytoband: 11q24.2
HGVS: NM_001134793.2(HYLS1):c.*262A>C
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.