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Variant (rsID / SNP)

rs1288401

SLC1A7

rs1288401 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC1A7. Location: chromosome 1, position 53,553,754. The table records no clinical significance for this variant.

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Reference-table entries

SLC1A7Not classified
Variant type
missense_variant
Chromosome / position
1:53553754
HGVS
NM_001287595.2,c.1787A>G,p.Gln596Arg
Allele change
Silent

Public references

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