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Variant (rsID / SNP)

rs1395

SLC5A6

rs1395 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC5A6. Location: chromosome 2, position 27,424,636. The table records no clinical significance for this variant.

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Reference-table entries

SLC5A6Not classified
Variant type
missense_variant
Chromosome / position
2:27424636
HGVS
NM_021095.4,c.1442C>T,p.Ser481Phe
Allele change
Missense_S481F

Associated conditions / phenotypes

Prostate Cancer

Public references

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