Variant (rsID / SNP)

rs142279599

rs142279599 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ETS1. Location: chromosome 11, position 128,354,963. Clinical significance in the table: Uncertain significance.

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Reference-table entries

ETS1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 11:128354963
Cytoband: 11q24.3
HGVS: NM_001143820.2(ETS1):c.617A>G (p.Tyr206Cys)
Allele change: Missense_Y162C

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.