Variant (rsID / SNP)

rs76315093

rs76315093 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC2A10. Location: chromosome 20, position 45,354,973. Clinical significance in the table: Benign.

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Reference-table entries

SLC2A10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 20:45354973
Cytoband: 20q13.12
HGVS: NM_030777.4(SLC2A10):c.1288+10G>A
Allele change: Silent

Associated conditions / phenotypes

Arterial tortuosity syndrome|Familial thoracic aortic aneurysm and aortic dissection

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.