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Variant (rsID / SNP)

rs1865760

SLC17A2

rs1865760 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC17A2. Location: chromosome 6, position 25,916,979. The table records no clinical significance for this variant.

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Reference-table entries

SLC17A2Not classified
Variant type
synonymous_variant
Chromosome / position
6:25916979
HGVS
NM_001286123.3,c.864G>A,p.Leu288Leu
Allele change
Synonymous_L288L

Public references

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