Variant (rsID / SNP)

rs140188939

rs140188939 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYROBP. Location: chromosome 19, position 36,398,158. Clinical significance in the table: Likely benign.

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Reference-table entries

TYROBPLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:36398158
Cytoband: 19q13.12
HGVS: NM_003332.4(TYROBP):c.238C>T (p.Arg80Trp)
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.