Variant (rsID / SNP)

rs10764687

rs10764687 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MASTL. Location: chromosome 10, position 27,475,579. Clinical significance in the table: Benign.

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Reference-table entries

MASTLBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:27475579
Cytoband: 10p12.1
HGVS: NM_001172303.3(MASTL):c.*114A>G
Allele change: Silent

Associated conditions / phenotypes

Thrombocytopenia

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.