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Variant (rsID / SNP)

rs748662135

SLC2A10

rs748662135 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC2A10. Location: chromosome 20, position 45,354,300. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SLC2A10Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
20:45354300
Cytoband
20q13.12
HGVS
NM_030777.4(SLC2A10):c.625C>T (p.Leu209=)
Allele change
Synonymous_L209L

Associated conditions / phenotypes

Arterial tortuosity syndrome|Cardiovascular phenotype

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.