Variant (rsID / SNP)

rs60639710

rs60639710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MIR181A1HG. Location: chromosome 1, position 198,867,678. Clinical significance in the table: Benign.

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Reference-table entries

MIR181A1HGBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:198867678
Cytoband: 1q32.1
HGVS: NR_040073.1(MIR181A1HG):n.363+1862C>A
Allele change: Silent

Associated conditions / phenotypes

Acute myeloblastic leukemia with maturation

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.